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rs63750745

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750745(-;-)
Make rs63750745(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993556
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63750745
ebirs63750745
HLIrs63750745
Exacrs63750745
Varsomers63750745
Maprs63750745
PheGenIrs63750745
hapmaprs63750745
1000 genomesrs63750745
hgdprs63750745
ensemblrs63750745
gopubmedrs63750745
geneviewrs63750745
scholarrs63750745
googlers63750745
pharmgkbrs63750745
gwascentralrs63750745
openSNPrs63750745
23andMers63750745
23andMe allrs63750745
SNP Nexus

SNPshotrs63750745
SNPdbers63750745
MSV3drs63750745
GWAS Ctlgrs63750745
Max Magnitude0
ClinVar
Risk rs63750745(;)
Alt rs63750745(;)
Reference rs63750745(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035047delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075957.2,