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rs876658918

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658918(-;-)
Make rs876658918(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47445615
GeneMSH2
is asnp
is mentioned by
dbSNPrs876658918
ebirs876658918
HLIrs876658918
Exacrs876658918
Varsomers876658918
Maprs876658918
PheGenIrs876658918
hapmaprs876658918
1000 genomesrs876658918
hgdprs876658918
ensemblrs876658918
gopubmedrs876658918
geneviewrs876658918
scholarrs876658918
googlers876658918
pharmgkbrs876658918
gwascentralrs876658918
openSNPrs876658918
23andMers876658918
23andMe allrs876658918
SNP Nexus

SNPshotrs876658918
SNPdbers876658918
MSV3drs876658918
GWAS Ctlgrs876658918
Max Magnitude0
ClinVar
Risk rs876658918(;)
Alt rs876658918(;)
Reference rs876658918(C;C)
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.47672754delC
CLNSRC
CLNACC RCV000222198.1,