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rs63749828

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63749828(-;-)
Make rs63749828(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993623
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63749828
ebirs63749828
HLIrs63749828
Exacrs63749828
Varsomers63749828
Maprs63749828
PheGenIrs63749828
hapmaprs63749828
1000 genomesrs63749828
hgdprs63749828
ensemblrs63749828
gopubmedrs63749828
geneviewrs63749828
scholarrs63749828
googlers63749828
pharmgkbrs63749828
gwascentralrs63749828
openSNPrs63749828
23andMers63749828
23andMe allrs63749828
SNP Nexus

SNPshotrs63749828
SNPdbers63749828
MSV3drs63749828
GWAS Ctlgrs63749828
Max Magnitude0
ClinVar
Risk rs63749828(;)
Alt rs63749828(;)
Reference rs63749828(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035114delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075839.2,