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rs63749804

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(I;I) 0
Make rs63749804(-;-)
Make rs63749804(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993599
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63749804
ebirs63749804
HLIrs63749804
Exacrs63749804
Varsomers63749804
Maprs63749804
PheGenIrs63749804
hapmaprs63749804
1000 genomesrs63749804
hgdprs63749804
ensemblrs63749804
gopubmedrs63749804
geneviewrs63749804
scholarrs63749804
googlers63749804
pharmgkbrs63749804
gwascentralrs63749804
openSNPrs63749804
23andMers63749804
23andMe allrs63749804
SNP Nexus

SNPshotrs63749804
SNPdbers63749804
MSV3drs63749804
GWAS Ctlgrs63749804
Max Magnitude0
ClinVar
Risk rs63749804(;)
Alt rs63749804(;)
Reference rs63749804(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035090delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075743.2,