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rs876659068

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659068(-;-)
Make rs876659068(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37047533
GeneMLH1
is asnp
is mentioned by
dbSNPrs876659068
ebirs876659068
HLIrs876659068
Exacrs876659068
Varsomers876659068
Maprs876659068
PheGenIrs876659068
hapmaprs876659068
1000 genomesrs876659068
hgdprs876659068
ensemblrs876659068
gopubmedrs876659068
geneviewrs876659068
scholarrs876659068
googlers876659068
pharmgkbrs876659068
gwascentralrs876659068
openSNPrs876659068
23andMers876659068
23andMe allrs876659068
SNP Nexus

SNPshotrs876659068
SNPdbers876659068
MSV3drs876659068
GWAS Ctlgrs876659068
Max Magnitude0
ClinVar
Risk rs876659068(;)
Alt rs876659068(;)
Reference rs876659068(C;C)
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.37089024delC
CLNSRC
CLNACC RCV000216550.1,