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rs876658915

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658915(C;C)
Make rs876658915(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37042298
GeneMLH1
is asnp
is mentioned by
dbSNPrs876658915
ebirs876658915
HLIrs876658915
Exacrs876658915
Varsomers876658915
Maprs876658915
PheGenIrs876658915
hapmaprs876658915
1000 genomesrs876658915
hgdprs876658915
ensemblrs876658915
gopubmedrs876658915
geneviewrs876658915
scholarrs876658915
googlers876658915
pharmgkbrs876658915
gwascentralrs876658915
openSNPrs876658915
23andMers876658915
23andMe allrs876658915
SNP Nexus

SNPshotrs876658915
SNPdbers876658915
MSV3drs876658915
GWAS Ctlgrs876658915
Max Magnitude0
ClinVar
Risk rs876658915(A,C;A,C)
Alt rs876658915(A,C;A,C)
Reference rs876658915(T;T)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37083789T>A; NC_000003.11:g.37083789T>C
CLNSRC
CLNACC RCV000214834.1, RCV000220192.1,