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rs63749813

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
(GA;GA) 0 common in clinvar
Make rs63749813(-;-)
Make rs63749813(-;GA)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993649
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63749813
ebirs63749813
HLIrs63749813
Exacrs63749813
Varsomers63749813
Maprs63749813
PheGenIrs63749813
hapmaprs63749813
1000 genomesrs63749813
hgdprs63749813
ensemblrs63749813
gopubmedrs63749813
geneviewrs63749813
scholarrs63749813
googlers63749813
pharmgkbrs63749813
gwascentralrs63749813
openSNPrs63749813
23andMers63749813
23andMe allrs63749813
SNP Nexus

SNPshotrs63749813
SNPdbers63749813
MSV3drs63749813
GWAS Ctlgrs63749813
Max Magnitude0
ClinVar
Risk rs63749813(;)
Alt rs63749813(;)
Reference rs63749813(AG;AG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035140_37035141delGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075078.2,