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rs63749816

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(I;I) 0
Make rs63749816(-;-)
Make rs63749816(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993578
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63749816
ebirs63749816
HLIrs63749816
Exacrs63749816
Varsomers63749816
Maprs63749816
PheGenIrs63749816
hapmaprs63749816
1000 genomesrs63749816
hgdprs63749816
ensemblrs63749816
gopubmedrs63749816
geneviewrs63749816
scholarrs63749816
googlers63749816
pharmgkbrs63749816
gwascentralrs63749816
openSNPrs63749816
23andMers63749816
23andMe allrs63749816
SNP Nexus

SNPshotrs63749816
SNPdbers63749816
MSV3drs63749816
GWAS Ctlgrs63749816
Max Magnitude0
ClinVar
Risk rs63749816(;)
Alt rs63749816(;)
Reference rs63749816(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035069delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075653.2,