IGF1R c.640+50199G>T

Variant ID: 15-99301535-G-T

NM_000875.3(IGF1R):c.640+50199G>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Epithelial-Mesenchymal Transition (EMT) Gene Variants and Epithelial Ovarian Cancer (EOC) Risk.

Genetic Epidemiology
Amankwah, Ernest K EK; Lin, Hui-Yi HY; Tyrer, Jonathan P JP; Lawrenson, Kate K; Dennis, Joe J; Chornokur, Ganna G; Aben, Katja K H KK; Anton-Culver, Hoda H; Antonenkova, Natalia N; Bruinsma, Fiona F; Bandera, Elisa V EV; Bean, Yukie T YT; Beckmann, Matthias W MW; Bisogna, Maria M; Bjorge, Line L; Bogdanova, Natalia N; Brinton, Louise A LA; Brooks-Wilson, Angela A; Bunker, Clareann H CH; Butzow, Ralf R; Campbell, Ian G IG; Carty, Karen K; Chen, Zhihua Z; Chen, Y Ann YA; Chang-Claude, Jenny J; Cook, Linda S LS; Cramer, Daniel W DW; Cunningham, Julie M JM; Cybulski, Cezary C; Dansonka-Mieszkowska, Agnieszka A; du Bois, Andreas A; Despierre, Evelyn E; Dicks, Ed E; Doherty, Jennifer A JA; Dörk, Thilo T; Dürst, Matthias M; Easton, Douglas F DF; Eccles, Diana M DM; Edwards, Robert P RP; Ekici, Arif B AB; Fasching, Peter A PA; Fridley, Brooke L BL; Gao, Yu-Tang YT; Gentry-Maharaj, Aleksandra A; Giles, Graham G GG; Glasspool, Rosalind R; Goodman, Marc T MT; Gronwald, Jacek J; Harrington, Patricia P; Harter, Philipp P; Hasmad, Hanis N HN; Hein, Alexander A; Heitz, Florian F; Hildebrandt, Michelle A T MA; Hillemanns, Peter P; Hogdall, Claus K CK; Hogdall, Estrid E; Hosono, Satoyo S; Iversen, Edwin S ES; Jakubowska, Anna A; Jensen, Allan A; Ji, Bu-Tian BT; Karlan, Beth Y BY; Jim, Heather H; Kellar, Melissa M; Kiemeney, Lambertus A LA; Krakstad, Camilla C; Kjaer, Susanne K SK; Kupryjanczyk, Jolanta J; Lambrechts, Diether D; Lambrechts, Sandrina S; Le, Nhu D ND; Lee, Alice W AW; Lele, Shashi S; Leminen, Arto A; Lester, Jenny J; Levine, Douglas A DA; Liang, Dong D; Lim, Boon Kiong BK; Lissowska, Jolanta J; Lu, Karen K; Lubinski, Jan J; Lundvall, Lene L; Massuger, Leon F A G LF; Matsuo, Keitaro K; McGuire, Valerie V; McLaughlin, John R JR; McNeish, Ian I; Menon, Usha U; Milne, Roger L RL; Modugno, Francesmary F; Moysich, Kirsten B KB; Ness, Roberta B RB; Nevanlinna, Heli H; Eilber, Ursula U; Odunsi, Kunle K; Olson, Sara H SH; Orlow, Irene I; Orsulic, Sandra S; Weber, Rachel Palmieri RP; Paul, James J; Pearce, Celeste L CL; Pejovic, Tanja T; Pelttari, Liisa M LM; Permuth-Wey, Jennifer J; Pike, Malcolm C MC; Poole, Elizabeth M EM; Risch, Harvey A HA; Rosen, Barry B; Rossing, Mary Anne MA; Rothstein, Joseph H JH; Rudolph, Anja A; Runnebaum, Ingo B IB; Rzepecka, Iwona K IK; Salvesen, Helga B HB; Schernhammer, Eva E; Schwaab, Ira I; Shu, Xiao-Ou XO; Shvetsov, Yurii B YB; Siddiqui, Nadeem N; Sieh, Weiva W; Song, Honglin H; Southey, Melissa C MC; Spiewankiewicz, Beata B; Sucheston-Campbell, Lara L; Teo, Soo-Hwang SH; Terry, Kathryn L KL; Thompson, Pamela J PJ; Thomsen, Lotte L; Tangen, Ingvild L IL; Tworoger, Shelley S SS; van Altena, Anne M AM; Vierkant, Robert A RA; Vergote, Ignace I; Walsh, Christine S CS; Wang-Gohrke, Shan S; Wentzensen, Nicolas N; Whittemore, Alice S AS; Wicklund, Kristine G KG; Wilkens, Lynne R LR; Wu, Anna H AH; Wu, Xifeng X; Woo, Yin-Ling YL; Yang, Hannah H; Zheng, Wei W; Ziogas, Argyrios A; Kelemen, Linda E LE; Berchuck, Andrew A; , ; Schildkraut, Joellen M JM; Ramus, Susan J SJ; Goode, Ellen L EL; Monteiro, Alvaro N A AN; Gayther, Simon A SA; Narod, Steven A SA; Pharoah, Paul D P PD; Sellers, Thomas A TA; Phelan, Catherine M CM
Publication Date: 2015-12

Variant appearance in text: rs10794486
PubMed Link: 26399219
Variant Present in the following documents:
  • Main text
View BVdb publication page



Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis.

Plos Genetics
Haataja, Ritva R; Karjalainen, Minna K MK; Luukkonen, Aino A; Teramo, Kari K; Puttonen, Hilkka H; Ojaniemi, Marja M; Varilo, Teppo T; Chaudhari, Bimal P BP; Plunkett, Jevon J; Murray, Jeffrey C JC; McCarroll, Steven A SA; Peltonen, Leena L; Muglia, Louis J LJ; Palotie, Aarno A; Hallman, Mikko M
Publication Date: 2011-02-03

Variant appearance in text: rs10794486
PubMed Link: 21304894
Variant Present in the following documents:
  • Main text
  • pgen.1001293.pdf
View BVdb publication page



Gene by smoking interaction in hypertension: identification of a major quantitative trait locus on chromosome 15q for systolic blood pressure in Mexican-Americans.

Journal Of Hypertension
Montasser, May E ME; Shimmin, Lawrence C LC; Hanis, Craig L CL; Boerwinkle, Eric E; Hixson, James E JE
Publication Date: 2009-03

Variant appearance in text: rs10794486
PubMed Link: 19330903
Variant Present in the following documents:
  • Main text
View BVdb publication page