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rs387906568

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906568(C;G)
Make rs387906568(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44909020
GeneAPOE
is asnp
is mentioned by
dbSNPrs387906568
ebirs387906568
HLIrs387906568
Exacrs387906568
Varsomers387906568
Maprs387906568
PheGenIrs387906568
hapmaprs387906568
1000 genomesrs387906568
hgdprs387906568
ensemblrs387906568
gopubmedrs387906568
geneviewrs387906568
scholarrs387906568
googlers387906568
pharmgkbrs387906568
gwascentralrs387906568
openSNPrs387906568
23andMers387906568
23andMe allrs387906568
SNP Nexus

SNPshotrs387906568
SNPdbers387906568
MSV3drs387906568
GWAS Ctlgrs387906568
Max Magnitude0
ClinVar
Risk rs387906568(G;G)
Alt rs387906568(G;G)
Reference rs387906568(C;C)
Significance Pathogenic
Disease Familial type 3 hyperlipoproteinemia
Variation info
Gene
CLNDBN Familial type 3 hyperlipoproteinemia
Reversed 0
HGVS NC_000019.9:g.45412277C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019452.2,