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rs267607790

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607790(A;A)
Make rs267607790(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37014546
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607790
ebirs267607790
HLIrs267607790
Exacrs267607790
Varsomers267607790
Maprs267607790
PheGenIrs267607790
hapmaprs267607790
1000 genomesrs267607790
hgdprs267607790
ensemblrs267607790
gopubmedrs267607790
geneviewrs267607790
scholarrs267607790
googlers267607790
pharmgkbrs267607790
gwascentralrs267607790
openSNPrs267607790
23andMers267607790
23andMe allrs267607790
SNP Nexus

SNPshotrs267607790
SNPdbers267607790
MSV3drs267607790
GWAS Ctlgrs267607790
Max Magnitude0
ClinVar
Risk rs267607790(A,C;A,C)
Alt rs267607790(A,C;A,C)
Reference rs267607790(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37056037T>A; NC_000003.11:g.37056037T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075850.2, RCV000075851.2,