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rs267607736

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607736(C;C)
Make rs267607736(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37004400
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607736
ebirs267607736
HLIrs267607736
Exacrs267607736
Varsomers267607736
Maprs267607736
PheGenIrs267607736
hapmaprs267607736
1000 genomesrs267607736
hgdprs267607736
ensemblrs267607736
gopubmedrs267607736
geneviewrs267607736
scholarrs267607736
googlers267607736
pharmgkbrs267607736
gwascentralrs267607736
openSNPrs267607736
23andMers267607736
23andMe allrs267607736
SNP Nexus

SNPshotrs267607736
SNPdbers267607736
MSV3drs267607736
GWAS Ctlgrs267607736
Max Magnitude0
ClinVar
Risk rs267607736(C;C)
Alt rs267607736(C;C)
Reference rs267607736(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37045891G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075641.2,