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rs267607854

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607854(A;A)
Make rs267607854(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047518
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607854
ebirs267607854
HLIrs267607854
Exacrs267607854
Varsomers267607854
Maprs267607854
PheGenIrs267607854
hapmaprs267607854
1000 genomesrs267607854
hgdprs267607854
ensemblrs267607854
gopubmedrs267607854
geneviewrs267607854
scholarrs267607854
googlers267607854
pharmgkbrs267607854
gwascentralrs267607854
openSNPrs267607854
23andMers267607854
23andMe allrs267607854
SNP Nexus

SNPshotrs267607854
SNPdbers267607854
MSV3drs267607854
GWAS Ctlgrs267607854
Max Magnitude0
ClinVar
Risk rs267607854(A;A)
Alt rs267607854(A;A)
Reference rs267607854(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089009G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075333.2,