CHEK2 c.847-1335G>T

Variant ID: 22-29100889-C-A

NM_007194.3(CHEK2):c.847-1335G>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Rare coding variants in DNA damage repair genes associated with timing of natural menopause.

Hgg Advances
Ward, Lucas D LD; Parker, Margaret M MM; Deaton, Aimee M AM; Tu, Ho-Chou HC; Flynn-Carroll, Alexander O AO; Hinkle, Gregory G; Nioi, Paul P
Publication Date: 2022-04-14

Variant appearance in text: rs12167378
PubMed Link: 35493704
Variant Present in the following documents:
  • mmc2.xlsx, sheet 10
View BVdb publication page