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rs876658223

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658223(G;T)
Make rs876658223(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47463034
GeneMSH2
is asnp
is mentioned by
dbSNPrs876658223
ebirs876658223
HLIrs876658223
Exacrs876658223
Varsomers876658223
Maprs876658223
PheGenIrs876658223
hapmaprs876658223
1000 genomesrs876658223
hgdprs876658223
ensemblrs876658223
gopubmedrs876658223
geneviewrs876658223
scholarrs876658223
googlers876658223
pharmgkbrs876658223
gwascentralrs876658223
openSNPrs876658223
23andMers876658223
23andMe allrs876658223
SNP Nexus

SNPshotrs876658223
SNPdbers876658223
MSV3drs876658223
GWAS Ctlgrs876658223
Max Magnitude0
ClinVar
Risk rs876658223(T;T)
Alt rs876658223(T;T)
Reference rs876658223(G;G)
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.47690173G>T
CLNSRC
CLNACC RCV000215886.1,