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rs876660386

From SNPedia

Orientationplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs876660386(ATTA;ATTA)
Make rs876660386(ATTA;TC)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47800055
GeneMSH6
is asnp
is mentioned by
dbSNPrs876660386
ebirs876660386
HLIrs876660386
Exacrs876660386
Varsomers876660386
Maprs876660386
PheGenIrs876660386
hapmaprs876660386
1000 genomesrs876660386
hgdprs876660386
ensemblrs876660386
gopubmedrs876660386
geneviewrs876660386
scholarrs876660386
googlers876660386
pharmgkbrs876660386
gwascentralrs876660386
openSNPrs876660386
23andMers876660386
23andMe allrs876660386
SNP Nexus

SNPshotrs876660386
SNPdbers876660386
MSV3drs876660386
GWAS Ctlgrs876660386
Max Magnitude0
ClinVar
Risk rs876660386(ATTA;ATTA)
Alt rs876660386(ATTA;ATTA)
Reference rs876660386(TC;TC)
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.48027194_48027195delTCinsATTA
CLNSRC
CLNACC RCV000220311.1,