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rs876660655

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876660655(-;-)
Make rs876660655(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47412499
GeneMSH2
is asnp
is mentioned by
dbSNPrs876660655
ebirs876660655
HLIrs876660655
Exacrs876660655
Varsomers876660655
Maprs876660655
PheGenIrs876660655
hapmaprs876660655
1000 genomesrs876660655
hgdprs876660655
ensemblrs876660655
gopubmedrs876660655
geneviewrs876660655
scholarrs876660655
googlers876660655
pharmgkbrs876660655
gwascentralrs876660655
openSNPrs876660655
23andMers876660655
23andMe allrs876660655
SNP Nexus

SNPshotrs876660655
SNPdbers876660655
MSV3drs876660655
GWAS Ctlgrs876660655
Max Magnitude0
ClinVar
Risk rs876660655(;)
Alt rs876660655(;)
Reference rs876660655(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.47639638delT
CLNSRC
CLNACC RCV000215038.1,