CARM1 c.669+464C>T

Variant ID: 19-11023434-C-T

NM_199141.1(CARM1):c.669+464C>T

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Identification of disease-associated loci using machine learning for genotype and network data integration.

Bioinformatics (Oxford, England)
Leal, Luis G LG; David, Alessia A; Jarvelin, Marjo-Riita MR; Sebert, Sylvain S; Männikkö, Minna M; Karhunen, Ville V; Seaby, Eleanor E; Hoggart, Clive C; Sternberg, Michael J E MJE
Publication Date: 2019-12-15

Variant appearance in text: rs1529711
PubMed Link: 31070705
Variant Present in the following documents:
  • Main text
  • btz310.pdf
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The effect of genetic variants on the relationship between statins and breast cancer in postmenopausal women in the Women's Health Initiative observational study.

Breast Cancer Research And Treatment
Bock, Cathryn H CH; Jay, Allison M AM; Dyson, Gregory G; Beebe-Dimmer, Jennifer L JL; Cote, Michele L ML; Hou, Lifang L; Howard, Barbara V BV; Desai, Pinkal P; Purrington, Kristen K; Prentice, Ross R; Simon, Michael S MS
Publication Date: 2018-02

Variant appearance in text: rs1529711
PubMed Link: 29063981
Variant Present in the following documents:
  • Main text
View BVdb publication page



Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation.

Bmc Genomics
Ligthart, Symen S; Vaez, Ahmad A; Hsu, Yi-Hsiang YH; , ; , ; , ; Stolk, Ronald R; Uitterlinden, André G AG; Hofman, Albert A; Alizadeh, Behrooz Z BZ; Franco, Oscar H OH; Dehghan, Abbas A
Publication Date: 2016-06-10

Variant appearance in text: rs1529711
PubMed Link: 27286809
Variant Present in the following documents:
  • Main text
  • 12864_2016_Article_2712.pdf
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Low-density lipoprotein receptor mutations generate synthetic genome-wide associations.

European Journal Of Human Genetics : Ejhg
Oosterveer, Daniëlla M DM; Versmissen, Jorie J; Defesche, Joep C JC; Sivapalaratnam, Suthesh S; Yazdanpanah, Mojgan M; Mulder, Monique M; van der Zee, Leonie L; Uitterlinden, André G AG; van Duijn, Cornelia M CM; Hofman, Albert A; Kastelein, John J P JJ; Aulchenko, Yurii S YS; Sijbrands, Eric J G EJ
Publication Date: 2013-05

Variant appearance in text: rs1529711
PubMed Link: 22968135
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: rs1529711
PubMed Link: 21269472
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genes encoding critical transcriptional activators for murine neural tube development and human spina bifida: a case-control study.

Bmc Medical Genetics
Lu, Wei W; Guzman, Adrian R AR; Yang, Wei W; Chapa, Claudia J CJ; Shaw, Gary M GM; Greene, Robert M RM; Pisano, M Michele MM; Lammer, Edward J EJ; Finnell, Richard H RH; Zhu, Huiping H
Publication Date: 2010-10-08

Variant appearance in text: rs1529711
PubMed Link: 20932315
Variant Present in the following documents:
  • Main text
  • 1471-2350-11-141.pdf
View BVdb publication page