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rs267607850

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607850(A;A)
Make rs267607850(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37042336
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607850
ebirs267607850
HLIrs267607850
Exacrs267607850
Varsomers267607850
Maprs267607850
PheGenIrs267607850
hapmaprs267607850
1000 genomesrs267607850
hgdprs267607850
ensemblrs267607850
gopubmedrs267607850
geneviewrs267607850
scholarrs267607850
googlers267607850
pharmgkbrs267607850
gwascentralrs267607850
openSNPrs267607850
23andMers267607850
23andMe allrs267607850
SNP Nexus

SNPshotrs267607850
SNPdbers267607850
MSV3drs267607850
GWAS Ctlgrs267607850
Max Magnitude0
ClinVar
Risk rs267607850(A;A)
Alt rs267607850(A;A)
Reference rs267607850(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37083827G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075328.2,