Have questions? Visit https://www.reddit.com/r/SNPedia

rs876658881

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658881(-;-)
Make rs876658881(-;A)
Make rs876658881(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47799502
GeneMSH6
is asnp
is mentioned by
dbSNPrs876658881
ebirs876658881
HLIrs876658881
Exacrs876658881
Varsomers876658881
Maprs876658881
PheGenIrs876658881
hapmaprs876658881
1000 genomesrs876658881
hgdprs876658881
ensemblrs876658881
gopubmedrs876658881
geneviewrs876658881
scholarrs876658881
googlers876658881
pharmgkbrs876658881
gwascentralrs876658881
openSNPrs876658881
23andMers876658881
23andMe allrs876658881
SNP Nexus

SNPshotrs876658881
SNPdbers876658881
MSV3drs876658881
GWAS Ctlgrs876658881
Max Magnitude0
ClinVar
Risk rs876658881(A;A)
Alt rs876658881(A;A)
Reference rs876658881(;)
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.48026641dupA
CLNSRC
CLNACC RCV000223287.1,