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rs876660546

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876660546(G;G)
Make rs876660546(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47480873
GeneMSH2
is asnp
is mentioned by
dbSNPrs876660546
ebirs876660546
HLIrs876660546
Exacrs876660546
Varsomers876660546
Maprs876660546
PheGenIrs876660546
hapmaprs876660546
1000 genomesrs876660546
hgdprs876660546
ensemblrs876660546
gopubmedrs876660546
geneviewrs876660546
scholarrs876660546
googlers876660546
pharmgkbrs876660546
gwascentralrs876660546
openSNPrs876660546
23andMers876660546
23andMe allrs876660546
SNP Nexus

SNPshotrs876660546
SNPdbers876660546
MSV3drs876660546
GWAS Ctlgrs876660546
Max Magnitude0
ClinVar
Risk rs876660546(G;G)
Alt rs876660546(G;G)
Reference rs876660546(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.47708012T>G
CLNSRC
CLNACC RCV000219827.1,