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rs876657701

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657701(C;T)
Make rs876657701(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47445655
GeneMSH2
is asnp
is mentioned by
dbSNPrs876657701
ebirs876657701
HLIrs876657701
Exacrs876657701
Varsomers876657701
Maprs876657701
PheGenIrs876657701
hapmaprs876657701
1000 genomesrs876657701
hgdprs876657701
ensemblrs876657701
gopubmedrs876657701
geneviewrs876657701
scholarrs876657701
googlers876657701
pharmgkbrs876657701
gwascentralrs876657701
openSNPrs876657701
23andMers876657701
23andMe allrs876657701
SNP Nexus

SNPshotrs876657701
SNPdbers876657701
MSV3drs876657701
GWAS Ctlgrs876657701
Max Magnitude0
ClinVar
Risk rs876657701(T;T)
Alt rs876657701(T;T)
Reference rs876657701(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47672794C>T
CLNSRC
CLNACC RCV000220084.1,