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rs267607710

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607710(C;C)
Make rs267607710(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993668
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs267607710
ebirs267607710
HLIrs267607710
Exacrs267607710
Varsomers267607710
Maprs267607710
PheGenIrs267607710
hapmaprs267607710
1000 genomesrs267607710
hgdprs267607710
ensemblrs267607710
gopubmedrs267607710
geneviewrs267607710
scholarrs267607710
googlers267607710
pharmgkbrs267607710
gwascentralrs267607710
openSNPrs267607710
23andMers267607710
23andMe allrs267607710
SNP Nexus

SNPshotrs267607710
SNPdbers267607710
MSV3drs267607710
GWAS Ctlgrs267607710
Max Magnitude0
ClinVar
Risk rs267607710(A,C;A,C)
Alt rs267607710(A,C;A,C)
Reference rs267607710(G;G)
Significance Pathogenic
Disease not specified Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN not specified Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035159G>A; NC_000003.11:g.37035159G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000202146.1, RCV000075129.2,