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rs267607786

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607786(A;G)
Make rs267607786(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37014548
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607786
ebirs267607786
HLIrs267607786
Exacrs267607786
Varsomers267607786
Maprs267607786
PheGenIrs267607786
hapmaprs267607786
1000 genomesrs267607786
hgdprs267607786
ensemblrs267607786
gopubmedrs267607786
geneviewrs267607786
scholarrs267607786
googlers267607786
pharmgkbrs267607786
gwascentralrs267607786
openSNPrs267607786
23andMers267607786
23andMe allrs267607786
SNP Nexus

SNPshotrs267607786
SNPdbers267607786
MSV3drs267607786
GWAS Ctlgrs267607786
Max Magnitude0
ClinVar
Risk rs267607786(C,G;C,G)
Alt rs267607786(C,G;C,G)
Reference rs267607786(A;A)
Significance Probable-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.37056039A>C; NC_000003.11:g.37056039A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000167140.1, RCV000075854.2,