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rs876658728

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658728(-;-)
Make rs876658728(-;T)
Make rs876658728(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47799042
GeneMSH6
is asnp
is mentioned by
dbSNPrs876658728
ebirs876658728
HLIrs876658728
Exacrs876658728
Varsomers876658728
Maprs876658728
PheGenIrs876658728
hapmaprs876658728
1000 genomesrs876658728
hgdprs876658728
ensemblrs876658728
gopubmedrs876658728
geneviewrs876658728
scholarrs876658728
googlers876658728
pharmgkbrs876658728
gwascentralrs876658728
openSNPrs876658728
23andMers876658728
23andMe allrs876658728
SNP Nexus

SNPshotrs876658728
SNPdbers876658728
MSV3drs876658728
GWAS Ctlgrs876658728
Max Magnitude0
ClinVar
Risk rs876658728(T;T)
Alt rs876658728(T;T)
Reference rs876658728(;)
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.48026181dupT
CLNSRC
CLNACC RCV000217160.1,