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rs63750792

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750792(C;T)
Make rs63750792(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993630
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63750792
ebirs63750792
HLIrs63750792
Exacrs63750792
Varsomers63750792
Maprs63750792
PheGenIrs63750792
hapmaprs63750792
1000 genomesrs63750792
hgdprs63750792
ensemblrs63750792
gopubmedrs63750792
geneviewrs63750792
scholarrs63750792
googlers63750792
pharmgkbrs63750792
gwascentralrs63750792
openSNPrs63750792
23andMers63750792
23andMe allrs63750792
SNP Nexus

SNPshotrs63750792
SNPdbers63750792
MSV3drs63750792
GWAS Ctlgrs63750792
Max Magnitude0
ClinVar
Risk rs63750792(T;T)
Alt rs63750792(T;T)
Reference rs63750792(C;C)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37035121C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075881.2, RCV000160552.2,