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