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rs267607739

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267607739(-;-)
Make rs267607739(-;A)
Make rs267607739(A;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37004440
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607739
ebirs267607739
HLIrs267607739
Exacrs267607739
Varsomers267607739
Maprs267607739
PheGenIrs267607739
hapmaprs267607739
1000 genomesrs267607739
hgdprs267607739
ensemblrs267607739
gopubmedrs267607739
geneviewrs267607739
scholarrs267607739
googlers267607739
pharmgkbrs267607739
gwascentralrs267607739
openSNPrs267607739
23andMers267607739
23andMe allrs267607739
SNP Nexus

SNPshotrs267607739
SNPdbers267607739
MSV3drs267607739
GWAS Ctlgrs267607739
Max Magnitude0
ClinVar
Risk rs267607739(A;A)
Alt rs267607739(A;A)
Reference rs267607739(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37045931dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075662.2,