rs387906568

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs387906568(C;G)

Make rs387906568(G;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

44909020

Gene

APOE

is a	snp
is	mentioned by
dbSNP	rs387906568
dbSNP (classic)	rs387906568
ClinGen	rs387906568
ebi	rs387906568
HLI	rs387906568
Exac	rs387906568
Gnomad	rs387906568
Varsome	rs387906568
LitVar	rs387906568
Map	rs387906568
PheGenI	rs387906568
Biobank	rs387906568
1000 genomes	rs387906568
hgdp	rs387906568
ensembl	rs387906568
geneview	rs387906568
scholar	rs387906568
google	rs387906568
pharmgkb	rs387906568
gwascentral	rs387906568
openSNP	rs387906568
23andMe	rs387906568
SNPshot	rs387906568
SNPdbe	rs387906568
MSV3d	rs387906568
GWAS Ctlg	rs387906568

Max Magnitude

0

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,