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rs267607743

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607743(A;G)
Make rs267607743(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37006989
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607743
ebirs267607743
HLIrs267607743
Exacrs267607743
Varsomers267607743
Maprs267607743
PheGenIrs267607743
hapmaprs267607743
1000 genomesrs267607743
hgdprs267607743
ensemblrs267607743
gopubmedrs267607743
geneviewrs267607743
scholarrs267607743
googlers267607743
pharmgkbrs267607743
gwascentralrs267607743
openSNPrs267607743
23andMers267607743
23andMe allrs267607743
SNP Nexus

SNPshotrs267607743
SNPdbers267607743
MSV3drs267607743
GWAS Ctlgrs267607743
Max Magnitude0
ClinVar
Risk rs267607743(G;G)
Alt rs267607743(G;G)
Reference rs267607743(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37048480A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075683.2,