PHF2 c.98+22769G>A

Variant ID: 9-96361922-G-A

NM_005392.3(PHF2):c.98+22769G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetically Predicted Insomnia in Relation to 14 Cardiovascular Conditions and 17 Cardiometabolic Risk Factors: A Mendelian Randomization Study.

Journal Of The American Heart Association
Liu, Xinhui X; Li, Chuanbao C; Sun, Xiaoru X; Yu, Yuanyuan Y; Si, Shucheng S; Hou, Lei L; Yan, Ran R; Yu, Yifan Y; Li, Mingzhuo M; Li, Hongkai H; Xue, Fuzhong F
Publication Date: 2021-08-03

Variant appearance in text: rs10761240
PubMed Link: 34315237
Variant Present in the following documents:
  • JAH3-10-e020187-s001.pdf
  • JAH3-10-e020187.pdf
View BVdb publication page