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rs63750823

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750823(G;T)
Make rs63750823(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993614
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63750823
ebirs63750823
HLIrs63750823
Exacrs63750823
Varsomers63750823
Maprs63750823
PheGenIrs63750823
hapmaprs63750823
1000 genomesrs63750823
hgdprs63750823
ensemblrs63750823
gopubmedrs63750823
geneviewrs63750823
scholarrs63750823
googlers63750823
pharmgkbrs63750823
gwascentralrs63750823
openSNPrs63750823
23andMers63750823
23andMe allrs63750823
SNP Nexus

SNPshotrs63750823
SNPdbers63750823
MSV3drs63750823
GWAS Ctlgrs63750823
Max Magnitude0
ClinVar
Risk rs63750823(A,T;A,T)
Alt rs63750823(A,T;A,T)
Reference rs63750823(G;G)
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.37035105G>A; NC_000003.11:g.37035105G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075821.2, RCV000075822.2, RCV000160551.1,