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rs876660549

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs876660549(-;-)
Make rs876660549(-;AA)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47799117
GeneMSH6
is asnp
is mentioned by
dbSNPrs876660549
ebirs876660549
HLIrs876660549
Exacrs876660549
Varsomers876660549
Maprs876660549
PheGenIrs876660549
hapmaprs876660549
1000 genomesrs876660549
hgdprs876660549
ensemblrs876660549
gopubmedrs876660549
geneviewrs876660549
scholarrs876660549
googlers876660549
pharmgkbrs876660549
gwascentralrs876660549
openSNPrs876660549
23andMers876660549
23andMe allrs876660549
SNP Nexus

SNPshotrs876660549
SNPdbers876660549
MSV3drs876660549
GWAS Ctlgrs876660549
Max Magnitude0
ClinVar
Risk rs876660549(;)
Alt rs876660549(;)
Reference rs876660549(AA;AA)
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.48026256_48026257delAA
CLNSRC
CLNACC RCV000217456.1,