CCND1 c.724-1093G>A

Variant ID: 11-69464793-G-A

NM_053056.2(CCND1):c.724-1093G>A

This variant was identified in 12 publications

View GRCh38 version.




Publications:


GWA-based pleiotropic analysis identified potential SNPs and genes related to type 2 diabetes and obesity.

Journal Of Human Genetics
Zeng, Yong Y; He, Hao H; Zhang, Lan L; Zhu, Wei W; Shen, Hui H; Yan, Yu-Jie YJ; Deng, Hong-Wen HW
Publication Date: 2021-03

Variant appearance in text: rs649392
PubMed Link: 32948839
Variant Present in the following documents:
  • Main text
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The CCND1 c.870G risk allele is enriched in individuals of African ancestry with plasma cell dyscrasias.

Blood Cancer Journal
Baughn, Linda B LB; Li, Zhuo Z; Pearce, Kathryn K; Vachon, Celine M CM; Polley, Mei-Yin MY; Keats, Jonathan J; Elhaik, Eran E; Baird, Michael M; Therneau, Terry T; Cerhan, James R JR; Bergsagel, P Leif PL; Dispenzieri, Angela A; Rajkumar, S Vincent SV; Asmann, Yan W YW; Kumar, Shaji S
Publication Date: 2020-03-16

Variant appearance in text: rs649392
PubMed Link: 32179748
Variant Present in the following documents:
  • Main text
  • 41408_2020_Article_294.pdf
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Polymorphisms and Pharmacogenomics for the Clinical Efficacy of Methotrexate in Patients with Rheumatoid Arthritis: A Systematic Review and Meta-analysis.

Scientific Reports
Qiu, Qi Q; Huang, Jing J; Shu, Xiaoming X; Fan, Huizheng H; Zhou, Youwen Y; Xiao, Cheng C
Publication Date: 2017-03-07

Variant appearance in text: rs649392
PubMed Link: 28266606
Variant Present in the following documents:
  • Main text
  • srep44015.pdf
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Polymorphisms near TBX5 and GDF7 are associated with increased risk for Barrett's esophagus.

Gastroenterology
Palles, Claire C; Chegwidden, Laura L; Li, Xinzhong X; Findlay, John M JM; Farnham, Garry G; Castro Giner, Francesc F; Peppelenbosch, Maikel P MP; Kovac, Michal M; Adams, Claire L CL; Prenen, Hans H; Briggs, Sarah S; Harrison, Rebecca R; Sanders, Scott S; MacDonald, David D; Haigh, Chris C; Tucker, Art A; Love, Sharon S; Nanji, Manoj M; deCaestecker, John J; Ferry, David D; Rathbone, Barrie B; Hapeshi, Julie J; Barr, Hugh H; Moayyedi, Paul P; Watson, Peter P; Zietek, Barbara B; Maroo, Neera N; Gay, Laura L; Underwood, Tim T; Boulter, Lisa L; McMurtry, Hugh H; Monk, David D; Patel, Praful P; Ragunath, Krish K; Al Dulaimi, David D; Murray, Iain I; Koss, Konrad K; Veitch, Andrew A; Trudgill, Nigel N; Nwokolo, Chuka C; Rembacken, Bjorn B; Atherfold, Paul P; Green, Elaine E; Ang, Yeng Y; Kuipers, Ernst J EJ; Chow, Wu W; Paterson, Stuart S; Kadri, Sudarshan S; Beales, Ian I; Grimley, Charles C; Mullins, Paul P; Beckett, Conrad C; Farrant, Mark M; Dixon, Andrew A; Kelly, Sean S; Johnson, Matthew M; Wajed, Shahjehan S; Dhar, Anjan A; Sawyer, Elinor E; Roylance, Rebecca R; Onstad, Lynn L; Gammon, Marilie D MD; Corley, Douglas A DA; Shaheen, Nicholas J NJ; Bird, Nigel C NC; Hardie, Laura J LJ; Reid, Brian J BJ; Ye, Weimin W; Liu, Geoffrey G; Romero, Yvonne Y; Bernstein, Leslie L; Wu, Anna H AH; Casson, Alan G AG; Fitzgerald, Rebecca R; Whiteman, David C DC; Risch, Harvey A HA; Levine, David M DM; Vaughan, Tom L TL; Verhaar, Auke P AP; van den Brande, Jan J; Toxopeus, Eelke L EL; Spaander, Manon C MC; Wijnhoven, Bas P L BP; van der Laan, Luc J W LJ; Krishnadath, Kausilia K; Wijmenga, Cisca C; Trynka, Gosia G; McManus, Ross R; Reynolds, John V JV; O'Sullivan, Jacintha J; MacMathuna, Padraic P; McGarrigle, Sarah A SA; Kelleher, Dermot D; Vermeire, Severine S; Cleynen, Isabelle I; Bisschops, Raf R; Tomlinson, Ian I; Jankowski, Janusz J
Publication Date: 2015-02

Variant appearance in text: rs649392
PubMed Link: 25447851
Variant Present in the following documents:
  • mmc1.pdf
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The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.

Nature Genetics
Weinhold, Niels N; Johnson, David C DC; Chubb, Daniel D; Chen, Bowang B; Försti, Asta A; Hosking, Fay J FJ; Broderick, Peter P; Ma, Yussanne P YP; Dobbins, Sara E SE; Hose, Dirk D; Walker, Brian A BA; Davies, Faith E FE; Kaiser, Martin F MF; Li, Ni L NL; Gregory, Walter A WA; Jackson, Graham H GH; Witzens-Harig, Mathias M; Neben, Kai K; Hoffmann, Per P; Nöthen, Markus M MM; Mühleisen, Thomas W TW; Eisele, Lewin L; Ross, Fiona M FM; Jauch, Anna A; Goldschmidt, Hartmut H; Houlston, Richard S RS; Morgan, Gareth J GJ; Hemminki, Kari K
Publication Date: 2013-05

Variant appearance in text: rs649392
PubMed Link: 23502783
Variant Present in the following documents:
  • Main text
  • NIHMS53125-supplement-1.pdf
  • emss-53125.pdf
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MicroRNA target site polymorphisms in the VHL-HIF1α pathway predict renal cell carcinoma risk.

Molecular Carcinogenesis
Wei, Hua H; Ke, Hung-Lung HL; Lin, Jie J; Shete, Sanjay S; Wood, Christopher G CG; Hildebrandt, Michelle A T MA
Publication Date: 2014-01

Variant appearance in text: rs649392
PubMed Link: 22517515
Variant Present in the following documents:
  • Main text
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Genetic variability in DNA repair and cell cycle control pathway genes and risk of smoking-related lung cancer.

Molecular Carcinogenesis
Buch, Shama C SC; Diergaarde, Brenda B; Nukui, Tomoko T; Day, Roger S RS; Siegfried, Jill M JM; Romkes, Marjorie M; Weissfeld, Joel L JL
Publication Date: 2012-10

Variant appearance in text: rs649392
PubMed Link: 21976407
Variant Present in the following documents:
  • Main text
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Genetic effects and modifiers of radiotherapy and chemotherapy on survival in pancreatic cancer.

Pancreas
Zeng, Hongmei H; Yu, Herbert H; Lu, Lingeng L; Jain, Dhanpat D; Kidd, Mark S MS; Saif, M Wasif MW; Chanock, Stephen J SJ; Hartge, Patricia P; , ; Risch, Harvey A HA
Publication Date: 2011-07

Variant appearance in text: rs649392
PubMed Link: 21487324
Variant Present in the following documents:
  • Main text
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Association of genetic polymorphisms in cell-cycle control genes and susceptibility to endometrial cancer among Chinese women.

American Journal Of Epidemiology
Cai, Hui H; Xiang, Yong-Bing YB; Qu, Shimian S; Long, Jirong J; Cai, Qiuyin Q; Gao, Jing J; Zheng, Wei W; Shu, Xiao Ou XO
Publication Date: 2011-06-01

Variant appearance in text: rs649392
PubMed Link: 21454826
Variant Present in the following documents:
  • Main text
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Genetic variation of ESR1 and its co-activator PPARGC1B is synergistic in augmenting the risk of estrogen receptor-positive breast cancer.

Breast Cancer Research : Bcr
Li, Yuqing Y; Li, Yi Y; Wedrén, Sara S; Li, Guoliang G; Charn, Tze Howe TH; Desai, Kartiki Vasant KV; Bonnard, Carine C; Czene, Kamila K; Humphreys, Keith K; Darabi, Hatef H; Einarsdóttir, Kristjana K; Heikkinen, Tuomas T; Aittomäki, Kristiina K; Blomqvist, Carl C; Chia, Kee Seng KS; Nevanlinna, Heli H; Hall, Per P; Liu, Edison T ET; Liu, Jianjun J
Publication Date: 2011-01-26

Variant appearance in text: rs649392
PubMed Link: 21269472
Variant Present in the following documents:
  • Main text
  • bcr2817.pdf
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Cell cycle genes and ovarian cancer susceptibility: a tagSNP analysis.

British Journal Of Cancer
Cunningham, J M JM; Vierkant, R A RA; Sellers, T A TA; Phelan, C C; Rider, D N DN; Liebow, M M; Schildkraut, J J; Berchuck, A A; Couch, F J FJ; Wang, X X; Fridley, B L BL; , ; Gentry-Maharaj, A A; Menon, U U; Hogdall, E E; Kjaer, S S; Whittemore, A A; DiCioccio, R R; Song, H H; Gayther, S A SA; Ramus, S J SJ; Pharaoh, P D P PD; Goode, E L EL
Publication Date: 2009-10-20

Variant appearance in text: rs649392
PubMed Link: 19738611
Variant Present in the following documents:
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Candidate gene analysis using imputed genotypes: cell cycle single-nucleotide polymorphisms and ovarian cancer risk.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Goode, Ellen L EL; Fridley, Brooke L BL; Vierkant, Robert A RA; Cunningham, Julie M JM; Phelan, Catherine M CM; Anderson, Stephanie S; Rider, David N DN; White, Kristin L KL; Pankratz, V Shane VS; Song, Honglin H; Hogdall, Estrid E; Kjaer, Susanne K SK; Whittemore, Alice S AS; DiCioccio, Richard R; Ramus, Susan J SJ; Gayther, Simon A SA; Schildkraut, Joellen M JM; Pharaoh, Paul P D PP; Sellers, Thomas A TA
Publication Date: 2009-03

Variant appearance in text: rs649392
PubMed Link: 19258477
Variant Present in the following documents:
  • Main text
View BVdb publication page