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rs876659068

From SNPedia

Orientationplus
Stabilizedplus
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
dbSNP (classic)rs876659068
ClinGenrs876659068
ebirs876659068
HLIrs876659068
Exacrs876659068
Gnomadrs876659068
Varsomers876659068
LitVarrs876659068
Maprs876659068
PheGenIrs876659068
Biobankrs876659068
1000 genomesrs876659068
hgdprs876659068
ensemblrs876659068
geneviewrs876659068
scholarrs876659068
googlers876659068
pharmgkbrs876659068
gwascentralrs876659068
openSNPrs876659068
23andMers876659068
SNPshotrs876659068
SNPdbers876659068
MSV3drs876659068
GWAS Ctlgrs876659068
Max Magnitude0
ClinVar
Risk rs876659068(-;-)
Alt rs876659068(-;-)
Reference Rs876659068(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37089024delC
CLNSRC
CLNACC RCV000216550.1,