F8 c.6430-14426G>T

Variant ID: X-154105928-C-A

NM_000132.3(F8):c.6430-14426G>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program.

American Journal Of Human Genetics
Sarnowski, Chloé C; Leong, Aaron A; Raffield, Laura M LM; Wu, Peitao P; de Vries, Paul S PS; DiCorpo, Daniel D; Guo, Xiuqing X; Xu, Huichun H; Liu, Yongmei Y; Zheng, Xiuwen X; Hu, Yao Y; Brody, Jennifer A JA; Goodarzi, Mark O MO; Hidalgo, Bertha A BA; Highland, Heather M HM; Jain, Deepti D; Liu, Ching-Ti CT; Naik, Rakhi P RP; O'Connell, Jeffrey R JR; Perry, James A JA; Porneala, Bianca C BC; Selvin, Elizabeth E; Wessel, Jennifer J; Psaty, Bruce M BM; Curran, Joanne E JE; Peralta, Juan M JM; Blangero, John J; Kooperberg, Charles C; Mathias, Rasika R; Johnson, Andrew D AD; Reiner, Alexander P AP; Mitchell, Braxton D BD; Cupples, L Adrienne LA; Vasan, Ramachandran S RS; Correa, Adolfo A; Morrison, Alanna C AC; Boerwinkle, Eric E; Rotter, Jerome I JI; Rich, Stephen S SS; Manning, Alisa K AK; Dupuis, Josée J; Meigs, James B JB; , ; , ; , ; ,
Publication Date: 2019-10-03

Variant appearance in text: rs189305788
PubMed Link: 31564435
Variant Present in the following documents:
  • Main text
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