Have questions? Visit https://www.reddit.com/r/SNPedia

rs267607745

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607745(A;A)
Make rs267607745(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37004475
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607745
ebirs267607745
HLIrs267607745
Exacrs267607745
Varsomers267607745
Maprs267607745
PheGenIrs267607745
hapmaprs267607745
1000 genomesrs267607745
hgdprs267607745
ensemblrs267607745
gopubmedrs267607745
geneviewrs267607745
scholarrs267607745
googlers267607745
pharmgkbrs267607745
gwascentralrs267607745
openSNPrs267607745
23andMers267607745
23andMe allrs267607745
SNP Nexus

SNPshotrs267607745
SNPdbers267607745
MSV3drs267607745
GWAS Ctlgrs267607745
Max Magnitude0
ClinVar
Risk rs267607745(A;A)
Alt rs267607745(A;A)
Reference rs267607745(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37045966G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075679.2,