FGD5 c.2659-2433G>T

Variant ID: 3-14919646-G-T

NM_152536.3(FGD5):c.2659-2433G>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Improved detection of common variants in coronary artery disease and blood pressure using a pleiotropy cFDR method.

Scientific Reports
Mao, Xiang-Jie XJ; Zhang, Qiang Q; Xu, Fei F; Gao, Pan P; Sun, Nan N; Wang, Bo B; Tang, Qi-Xin QX; Hao, Yi-Bin YB; Sun, Chang-Qing CQ
Publication Date: 2019-07-17

Variant appearance in text: rs13070927
PubMed Link: 31316127
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors.

Multiple Sclerosis (Houndmills, Basingstoke, England)
Wang, Yunpeng Y; Bos, Steffan D SD; Harbo, Hanne F HF; Thompson, Wesley K WK; Schork, Andrew J AJ; Bettella, Francesco F; Witoelar, Aree A; Lie, Benedicte A BA; Li, Wen W; McEvoy, Linda K LK; Djurovic, Srdjan S; Desikan, Rahul S RS; Dale, Anders M AM; Andreassen, Ole A OA
Publication Date: 2016-12

Variant appearance in text: rs13070927
PubMed Link: 26920376
Variant Present in the following documents:
  • Main text
View BVdb publication page