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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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