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rs876659961

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659961(CA;CA)
Make rs876659961(CA;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47475269
GeneMSH2
is asnp
is mentioned by
dbSNPrs876659961
ebirs876659961
HLIrs876659961
Exacrs876659961
Varsomers876659961
Maprs876659961
PheGenIrs876659961
hapmaprs876659961
1000 genomesrs876659961
hgdprs876659961
ensemblrs876659961
gopubmedrs876659961
geneviewrs876659961
scholarrs876659961
googlers876659961
pharmgkbrs876659961
gwascentralrs876659961
openSNPrs876659961
23andMers876659961
23andMe allrs876659961
SNP Nexus

SNPshotrs876659961
SNPdbers876659961
MSV3drs876659961
GWAS Ctlgrs876659961
Max Magnitude0
ClinVar
Risk rs876659961(CA;CA)
Alt rs876659961(CA;CA)
Reference rs876659961(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.47702408delTinsCA
CLNSRC
CLNACC RCV000215947.1,