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rs267607784

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607784(C;G)
Make rs267607784(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37014431
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607784
ebirs267607784
HLIrs267607784
Exacrs267607784
Varsomers267607784
Maprs267607784
PheGenIrs267607784
hapmaprs267607784
1000 genomesrs267607784
hgdprs267607784
ensemblrs267607784
gopubmedrs267607784
geneviewrs267607784
scholarrs267607784
googlers267607784
pharmgkbrs267607784
gwascentralrs267607784
openSNPrs267607784
23andMers267607784
23andMe allrs267607784
SNP Nexus

SNPshotrs267607784
SNPdbers267607784
MSV3drs267607784
GWAS Ctlgrs267607784
Max Magnitude0
ClinVar
Risk rs267607784(A,G;A,G)
Alt rs267607784(A,G;A,G)
Reference rs267607784(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000003.11:g.37055922G>C; NC_000003.11:g.37055922G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075813.2, RCV000075814.2,