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rs876659608

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659608(G;T)
Make rs876659608(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37050588
GeneMLH1
is asnp
is mentioned by
dbSNPrs876659608
ebirs876659608
HLIrs876659608
Exacrs876659608
Varsomers876659608
Maprs876659608
PheGenIrs876659608
hapmaprs876659608
1000 genomesrs876659608
hgdprs876659608
ensemblrs876659608
gopubmedrs876659608
geneviewrs876659608
scholarrs876659608
googlers876659608
pharmgkbrs876659608
gwascentralrs876659608
openSNPrs876659608
23andMers876659608
23andMe allrs876659608
SNP Nexus

SNPshotrs876659608
SNPdbers876659608
MSV3drs876659608
GWAS Ctlgrs876659608
Max Magnitude0
ClinVar
Risk rs876659608(T;T)
Alt rs876659608(T;T)
Reference rs876659608(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37092079G>T
CLNSRC
CLNACC RCV000219289.1,