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MSH2 c.1386+7377G>T
Variant ID: 2-47680173-G-T
NM_000251.2(
MSH2
):c.1386+7377G>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:
Unique DNA repair gene variations and potential associations with the primary antibody deficiency syndromes IgAD and CVID.
Plos One
Offer, Steven M SM; Pan-Hammarström, Qiang Q; Hammarström, Lennart L; Harris, Reuben S RS
Publication Date: 2010-08-18
Variant appearance in text: rs3771276
PubMed Link:
20805886
Variant Present in the following documents:
Main text
pone.0012260.pdf
View BVdb publication page