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rs876658940

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658940(-;-)
Make rs876658940(-;A)
Make rs876658940(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47475047
GeneMSH2
is asnp
is mentioned by
dbSNPrs876658940
ebirs876658940
HLIrs876658940
Exacrs876658940
Varsomers876658940
Maprs876658940
PheGenIrs876658940
hapmaprs876658940
1000 genomesrs876658940
hgdprs876658940
ensemblrs876658940
gopubmedrs876658940
geneviewrs876658940
scholarrs876658940
googlers876658940
pharmgkbrs876658940
gwascentralrs876658940
openSNPrs876658940
23andMers876658940
23andMe allrs876658940
SNP Nexus

SNPshotrs876658940
SNPdbers876658940
MSV3drs876658940
GWAS Ctlgrs876658940
Max Magnitude0
ClinVar
Risk rs876658940(A;A)
Alt rs876658940(A;A)
Reference rs876658940(;)
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.47702186dupA
CLNSRC
CLNACC RCV000214939.1,