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rs267607716

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607716(A;G)
Make rs267607716(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37000953
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607716
ebirs267607716
HLIrs267607716
Exacrs267607716
Varsomers267607716
Maprs267607716
PheGenIrs267607716
hapmaprs267607716
1000 genomesrs267607716
hgdprs267607716
ensemblrs267607716
gopubmedrs267607716
geneviewrs267607716
scholarrs267607716
googlers267607716
pharmgkbrs267607716
gwascentralrs267607716
openSNPrs267607716
23andMers267607716
23andMe allrs267607716
SNP Nexus

SNPshotrs267607716
SNPdbers267607716
MSV3drs267607716
GWAS Ctlgrs267607716
Max Magnitude0
ClinVar
Risk rs267607716(C,G;C,G)
Alt rs267607716(C,G;C,G)
Reference rs267607716(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene MLH1
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37042444A>C; NC_000003.11:g.37042444A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000165647.1, RCV000075516.2,