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rs267607732

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;C) 6 Lynch syndrome, pathogenic mutation
Make rs267607732(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37004399
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607732
dbSNP (old)rs267607732
ClinGenrs267607732
ebirs267607732
HLIrs267607732
Exacrs267607732
Gnomadrs267607732
Varsomers267607732
Maprs267607732
PheGenIrs267607732
Biobankrs267607732
1000 genomesrs267607732
hgdprs267607732
ensemblrs267607732
gopubmedrs267607732
geneviewrs267607732
scholarrs267607732
googlers267607732
pharmgkbrs267607732
gwascentralrs267607732
openSNPrs267607732
23andMers267607732
23andMe allrs267607732
SNPshotrs267607732
SNPdbers267607732
MSV3drs267607732
GWAS Ctlgrs267607732
Max Magnitude6
ClinVar
Risk rs267607732(C;C) rs267607732(G;G)
Alt rs267607732(C;C) rs267607732(G;G)
Reference Rs267607732(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37045890A>C; NC_000003.11:g.37045890A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075644.2, RCV000214340.1,