IGF1R c.640+11938T>C

Variant ID: 15-99263274-T-C

NM_000875.3(IGF1R):c.640+11938T>C

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Integrated genetic analyses revealed novel human longevity loci and reduced risks of multiple diseases in a cohort study of 15,651 Chinese individuals.

Aging Cell
Liu, Xiaomin X; Song, Zijun Z; Li, Yan Y; Yao, Yao Y; Fang, Mingyan M; Bai, Chen C; An, Peng P; Chen, Huashuai H; Chen, Zhihua Z; Tang, Biyao B; Shen, Juan J; Gao, Xiaotong X; Zhang, Mingrong M; Chen, Pengyu P; Zhang, Tao T; Jia, Huijue H; Liu, Xiao X; Hou, Yong Y; Yang, Huanming H; Wang, Jian J; Wang, Fudi F; Xu, Xun X; Min, Junxia J; Nie, Chao C; Zeng, Yi Y
Publication Date: 2021-03

Variant appearance in text: rs8038015
PubMed Link: 33657282
Variant Present in the following documents:
  • ACEL-20-e13323-s014.xlsx, sheet 1
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Systemic Investigation of Promoter-wide Methylome and Genome Variations in Gout.

International Journal Of Molecular Sciences
Tseng, Chia-Chun CC; Wong, Man Chun MC; Liao, Wei-Ting WT; Chen, Chung-Jen CJ; Lee, Su-Chen SC; Yen, Jeng-Hsien JH; Chang, Shun-Jen SJ
Publication Date: 2020-07-01

Variant appearance in text: rs8038015
PubMed Link: 32630231
Variant Present in the following documents:
  • ijms-21-04702-s001.pdf
View BVdb publication page



Sequence variants with large effects on cardiac electrophysiology and disease.

Nature Communications
Norland, Kristjan K; Sveinbjornsson, Gardar G; Thorolfsdottir, Rosa B RB; Davidsson, Olafur B OB; Tragante, Vinicius V; Rajamani, Sridharan S; Helgadottir, Anna A; Gretarsdottir, Solveig S; van Setten, Jessica J; Asselbergs, Folkert W FW; Sverrisson, Jon Th JT; Stephensen, Sigurdur S SS; Oskarsson, Gylfi G; Sigurdsson, Emil L EL; Andersen, Karl K; Danielsen, Ragnar R; Thorgeirsson, Gudmundur G; Thorsteinsdottir, Unnur U; Arnar, David O DO; Sulem, Patrick P; Holm, Hilma H; Gudbjartsson, Daniel F DF; Stefansson, Kari K
Publication Date: 2019-10-22

Variant appearance in text: rs8038015
PubMed Link: 31641117
Variant Present in the following documents:
  • 41467_2019_12682_MOESM2_ESM.pdf
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Guided exploration of genomic risk for gray matter abnormalities in schizophrenia using parallel independent component analysis with reference.

Neuroimage
Chen, Jiayu J; Calhoun, Vince D VD; Pearlson, Godfrey D GD; Perrone-Bizzozero, Nora N; Sui, Jing J; Turner, Jessica A JA; Bustillo, Juan R JR; Ehrlich, Stefan S; Sponheim, Scott R SR; Cañive, José M JM; Ho, Beng-Choon BC; Liu, Jingyu J
Publication Date: 2013-12

Variant appearance in text: rs8038015
PubMed Link: 23727316
Variant Present in the following documents:
  • Main text
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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: rs8038015
PubMed Link: 19330903
Variant Present in the following documents:
  • Main text
View BVdb publication page