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rs267607709

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607709(A;A)
Make rs267607709(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993664
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs267607709
ebirs267607709
HLIrs267607709
Exacrs267607709
Varsomers267607709
Maprs267607709
PheGenIrs267607709
hapmaprs267607709
1000 genomesrs267607709
hgdprs267607709
ensemblrs267607709
gopubmedrs267607709
geneviewrs267607709
scholarrs267607709
googlers267607709
pharmgkbrs267607709
gwascentralrs267607709
openSNPrs267607709
23andMers267607709
23andMe allrs267607709
SNP Nexus

SNPshotrs267607709
SNPdbers267607709
MSV3drs267607709
GWAS Ctlgrs267607709
Max Magnitude0
ClinVar
Risk rs267607709(A;A)
Alt rs267607709(A;A)
Reference rs267607709(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035155G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075127.2,