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MSH2 c.1277-2297G>A
Variant ID: 2-47670390-G-A
NM_000251.2(
MSH2
):c.1277-2297G>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:
Inversion of exons 1-7 of the MSH2 gene is a frequent cause of unexplained Lynch syndrome in one local population.
Familial Cancer
Rhees, Jennifer J; Arnold, Mildred M; Boland, C Richard CR
Publication Date: 2014-06
Variant appearance in text: rs6726832
PubMed Link:
24114314
Variant Present in the following documents:
Main text
View BVdb publication page