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rs267607702

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GTTATTCGGCGGCTGGA;GTTATTCGGCGGCTGGA) 0 common in clinvar
Make rs267607702(-;-)
Make rs267607702(-;GTTATTCGGCGGCTGGA)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993566
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs267607702
dbSNP (old)rs267607702
ClinGenrs267607702
ebirs267607702
HLIrs267607702
Exacrs267607702
Varsomers267607702
Maprs267607702
PheGenIrs267607702
Biobankrs267607702
1000 genomesrs267607702
hgdprs267607702
ensemblrs267607702
gopubmedrs267607702
geneviewrs267607702
scholarrs267607702
googlers267607702
pharmgkbrs267607702
gwascentralrs267607702
openSNPrs267607702
23andMers267607702
23andMe allrs267607702
SNP Nexus

SNPshotrs267607702
SNPdbers267607702
MSV3drs267607702
GWAS Ctlgrs267607702
Max Magnitude0
ClinVar
Risk rs267607702(-;-)
Alt rs267607702(-;-)
Reference Rs267607702(GTTATTCGGCGGCTGGA;GTTATTCGGCGGCTGGA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035057_37035073del17
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075476.2,