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rs876658604

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658604(-;-)
Make rs876658604(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47799881
GeneMSH6
is asnp
is mentioned by
dbSNPrs876658604
ebirs876658604
HLIrs876658604
Exacrs876658604
Varsomers876658604
Maprs876658604
PheGenIrs876658604
hapmaprs876658604
1000 genomesrs876658604
hgdprs876658604
ensemblrs876658604
gopubmedrs876658604
geneviewrs876658604
scholarrs876658604
googlers876658604
pharmgkbrs876658604
gwascentralrs876658604
openSNPrs876658604
23andMers876658604
23andMe allrs876658604
SNP Nexus

SNPshotrs876658604
SNPdbers876658604
MSV3drs876658604
GWAS Ctlgrs876658604
Max Magnitude0
ClinVar
Risk rs876658604(;)
Alt rs876658604(;)
Reference rs876658604(C;C)
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.48027020delC
CLNSRC
CLNACC RCV000221157.1,