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rs876660095

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660095(G;T)
Make rs876660095(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47783236
GeneMSH6
is asnp
is mentioned by
dbSNPrs876660095
ebirs876660095
HLIrs876660095
Exacrs876660095
Varsomers876660095
Maprs876660095
PheGenIrs876660095
hapmaprs876660095
1000 genomesrs876660095
hgdprs876660095
ensemblrs876660095
gopubmedrs876660095
geneviewrs876660095
scholarrs876660095
googlers876660095
pharmgkbrs876660095
gwascentralrs876660095
openSNPrs876660095
23andMers876660095
23andMe allrs876660095
SNP Nexus

SNPshotrs876660095
SNPdbers876660095
MSV3drs876660095
GWAS Ctlgrs876660095
Max Magnitude0
ClinVar
Risk rs876660095(T;T)
Alt rs876660095(T;T)
Reference rs876660095(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.48010375G>T
CLNSRC
CLNACC RCV000219646.1,