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rs63749839

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63749839(-;-)
Make rs63749839(-;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993620
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63749839
ebirs63749839
HLIrs63749839
Exacrs63749839
Varsomers63749839
Maprs63749839
PheGenIrs63749839
hapmaprs63749839
1000 genomesrs63749839
hgdprs63749839
ensemblrs63749839
gopubmedrs63749839
geneviewrs63749839
scholarrs63749839
googlers63749839
pharmgkbrs63749839
gwascentralrs63749839
openSNPrs63749839
23andMers63749839
23andMe allrs63749839
SNP Nexus

SNPshotrs63749839
SNPdbers63749839
MSV3drs63749839
GWAS Ctlgrs63749839
Max Magnitude0
ClinVar
Risk rs63749839(;)
Alt rs63749839(;)
Reference rs63749839(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035111delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075835.2,