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rs267607751

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607751(C;C)
Make rs267607751(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37007065
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607751
ebirs267607751
HLIrs267607751
Exacrs267607751
Varsomers267607751
Maprs267607751
PheGenIrs267607751
hapmaprs267607751
1000 genomesrs267607751
hgdprs267607751
ensemblrs267607751
gopubmedrs267607751
geneviewrs267607751
scholarrs267607751
googlers267607751
pharmgkbrs267607751
gwascentralrs267607751
openSNPrs267607751
23andMers267607751
23andMe allrs267607751
SNP Nexus

SNPshotrs267607751
SNPdbers267607751
MSV3drs267607751
GWAS Ctlgrs267607751
Max Magnitude0
ClinVar
Risk rs267607751(C;C)
Alt rs267607751(C;C)
Reference rs267607751(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37048556T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075713.2,