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rs267607729

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267607729(-;-)
Make rs267607729(-;A)
Make rs267607729(A;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37000991
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607729
ebirs267607729
HLIrs267607729
Exacrs267607729
Varsomers267607729
Maprs267607729
PheGenIrs267607729
hapmaprs267607729
1000 genomesrs267607729
hgdprs267607729
ensemblrs267607729
gopubmedrs267607729
geneviewrs267607729
scholarrs267607729
googlers267607729
pharmgkbrs267607729
gwascentralrs267607729
openSNPrs267607729
23andMers267607729
23andMe allrs267607729
SNP Nexus

SNPshotrs267607729
SNPdbers267607729
MSV3drs267607729
GWAS Ctlgrs267607729
Max Magnitude0
ClinVar
Risk rs267607729(A;A)
Alt rs267607729(A;A)
Reference rs267607729(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37042482dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075603.2,