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rs63750580

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63750580(A;G)
Make rs63750580(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993659
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63750580
ebirs63750580
HLIrs63750580
Exacrs63750580
Varsomers63750580
Maprs63750580
PheGenIrs63750580
hapmaprs63750580
1000 genomesrs63750580
hgdprs63750580
ensemblrs63750580
gopubmedrs63750580
geneviewrs63750580
scholarrs63750580
googlers63750580
pharmgkbrs63750580
gwascentralrs63750580
openSNPrs63750580
23andMers63750580
23andMe allrs63750580
SNP Nexus

SNPshotrs63750580
SNPdbers63750580
MSV3drs63750580
GWAS Ctlgrs63750580
Max Magnitude0
ClinVar
Risk rs63750580(C,G;C,G)
Alt rs63750580(C,G;C,G)
Reference rs63750580(A;A)
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.37035150A>C; NC_000003.11:g.37035150A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075115.2, RCV000129232.2, RCV000075116.2,