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rs876659073

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659073(-;-)
Make rs876659073(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37020461
GeneMLH1
is asnp
is mentioned by
dbSNPrs876659073
ClinGenrs876659073
ebirs876659073
HLIrs876659073
Exacrs876659073
Varsomers876659073
Maprs876659073
PheGenIrs876659073
hapmaprs876659073
1000 genomesrs876659073
hgdprs876659073
ensemblrs876659073
gopubmedrs876659073
geneviewrs876659073
scholarrs876659073
googlers876659073
pharmgkbrs876659073
gwascentralrs876659073
openSNPrs876659073
23andMers876659073
23andMe allrs876659073
SNP Nexus

SNPshotrs876659073
SNPdbers876659073
MSV3drs876659073
GWAS Ctlgrs876659073
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs876659073(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.37061952delC
CLNSRC
CLNACC RCV000216790.1,