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rs63750581

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750581(-;-)
Make rs63750581(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993608
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63750581
ebirs63750581
HLIrs63750581
Exacrs63750581
Varsomers63750581
Maprs63750581
PheGenIrs63750581
hapmaprs63750581
1000 genomesrs63750581
hgdprs63750581
ensemblrs63750581
gopubmedrs63750581
geneviewrs63750581
scholarrs63750581
googlers63750581
pharmgkbrs63750581
gwascentralrs63750581
openSNPrs63750581
23andMers63750581
23andMe allrs63750581
SNP Nexus

SNPshotrs63750581
SNPdbers63750581
MSV3drs63750581
GWAS Ctlgrs63750581
Max Magnitude0
ClinVar
Risk rs63750581(;)
Alt rs63750581(;)
Reference rs63750581(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035099delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075785.2,