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rs876660037

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660037(A;A)
Make rs876660037(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47800314
GeneMSH6
is asnp
is mentioned by
dbSNPrs876660037
ebirs876660037
HLIrs876660037
Exacrs876660037
Varsomers876660037
Maprs876660037
PheGenIrs876660037
hapmaprs876660037
1000 genomesrs876660037
hgdprs876660037
ensemblrs876660037
gopubmedrs876660037
geneviewrs876660037
scholarrs876660037
googlers876660037
pharmgkbrs876660037
gwascentralrs876660037
openSNPrs876660037
23andMers876660037
23andMe allrs876660037
SNP Nexus

SNPshotrs876660037
SNPdbers876660037
MSV3drs876660037
GWAS Ctlgrs876660037
Max Magnitude0
ClinVar
Risk rs876660037(A;A)
Alt rs876660037(A;A)
Reference rs876660037(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH6
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.48027453G>A
CLNSRC
CLNACC RCV000214405.1,