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rs876659189

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659189(-;-)
Make rs876659189(-;TT)
Make rs876659189(TT;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47800788
GeneMSH6
is asnp
is mentioned by
dbSNPrs876659189
ebirs876659189
HLIrs876659189
Exacrs876659189
Varsomers876659189
Maprs876659189
PheGenIrs876659189
hapmaprs876659189
1000 genomesrs876659189
hgdprs876659189
ensemblrs876659189
gopubmedrs876659189
geneviewrs876659189
scholarrs876659189
googlers876659189
pharmgkbrs876659189
gwascentralrs876659189
openSNPrs876659189
23andMers876659189
23andMe allrs876659189
SNP Nexus

SNPshotrs876659189
SNPdbers876659189
MSV3drs876659189
GWAS Ctlgrs876659189
Max Magnitude0
ClinVar
Risk rs876659189(TT;TT)
Alt rs876659189(TT;TT)
Reference rs876659189(;)
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.48027927_48027928insTT
CLNSRC
CLNACC RCV000218854.1,