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rs267607738

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267607738(-;-)
Make rs267607738(-;T)
Make rs267607738(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37001055
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607738
ebirs267607738
HLIrs267607738
Exacrs267607738
Varsomers267607738
Maprs267607738
PheGenIrs267607738
hapmaprs267607738
1000 genomesrs267607738
hgdprs267607738
ensemblrs267607738
gopubmedrs267607738
geneviewrs267607738
scholarrs267607738
googlers267607738
pharmgkbrs267607738
gwascentralrs267607738
openSNPrs267607738
23andMers267607738
23andMe allrs267607738
SNP Nexus

SNPshotrs267607738
SNPdbers267607738
MSV3drs267607738
GWAS Ctlgrs267607738
Max Magnitude0
ClinVar
Risk rs267607738(T;T)
Alt rs267607738(T;T)
Reference rs267607738(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37042546dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075629.2,