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rs267607726

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 6 Lynch syndrome, pathogenic mutation
(G;G) 0 common in clinvar


Make rs267607726(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position37001048
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607726
dbSNP (old)rs267607726
ClinGenrs267607726
ebirs267607726
HLIrs267607726
Exacrs267607726
Gnomadrs267607726
Varsomers267607726
Maprs267607726
PheGenIrs267607726
Biobankrs267607726
1000 genomesrs267607726
hgdprs267607726
ensemblrs267607726
gopubmedrs267607726
geneviewrs267607726
scholarrs267607726
googlers267607726
pharmgkbrs267607726
gwascentralrs267607726
openSNPrs267607726
23andMers267607726
23andMe allrs267607726
SNPshotrs267607726
SNPdbers267607726
MSV3drs267607726
GWAS Ctlgrs267607726
Max Magnitude6
ClinVar
Risk rs267607726(A;A)
Alt rs267607726(A;A)
Reference Rs267607726(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome I not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome I not provided
Reversed 0
HGVS NC_000003.11:g.37042539G>A
CLNSRC UniProtKB (protein)
CLNACC RCV000075623.2, RCV000486320.1,