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rs267607722

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607722(C;C)
Make rs267607722(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996711
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607722
ebirs267607722
HLIrs267607722
Exacrs267607722
Varsomers267607722
Maprs267607722
PheGenIrs267607722
hapmaprs267607722
1000 genomesrs267607722
hgdprs267607722
ensemblrs267607722
gopubmedrs267607722
geneviewrs267607722
scholarrs267607722
googlers267607722
pharmgkbrs267607722
gwascentralrs267607722
openSNPrs267607722
23andMers267607722
23andMe allrs267607722
SNP Nexus

SNPshotrs267607722
SNPdbers267607722
MSV3drs267607722
GWAS Ctlgrs267607722
Max Magnitude0
ClinVar
Risk rs267607722(C;C)
Alt rs267607722(C;C)
Reference rs267607722(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038202T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075508.2,