Have questions? Visit https://www.reddit.com/r/SNPedia

rs397514253

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397514253(A;G)
Make rs397514253(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44908531
GeneAPOE
is asnp
is mentioned by
dbSNPrs397514253
ebirs397514253
HLIrs397514253
Exacrs397514253
Varsomers397514253
Maprs397514253
PheGenIrs397514253
hapmaprs397514253
1000 genomesrs397514253
hgdprs397514253
ensemblrs397514253
gopubmedrs397514253
geneviewrs397514253
scholarrs397514253
googlers397514253
pharmgkbrs397514253
gwascentralrs397514253
openSNPrs397514253
23andMers397514253
23andMe allrs397514253
SNP Nexus

SNPshotrs397514253
SNPdbers397514253
MSV3drs397514253
GWAS Ctlgrs397514253
Max Magnitude0
ClinVar
Risk rs397514253(G;G)
Alt rs397514253(G;G)
Reference rs397514253(A;A)
Significance Pathogenic
Disease Familial type 3 hyperlipoproteinemia
Variation info
Gene APOE
CLNDBN Familial type 3 hyperlipoproteinemia
Reversed 0
HGVS NC_000019.9:g.45411788A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019433.27,