rs201672011

Orientation

plus

Stabilized

plus

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

Make rs201672011(A;A)

Make rs201672011(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

44907807

Gene

APOE

is a	snp
is	mentioned by
dbSNP	rs201672011
dbSNP (classic)	rs201672011
ClinGen	rs201672011
ebi	rs201672011
HLI	rs201672011
Exac	rs201672011
Gnomad	rs201672011
Varsome	rs201672011
LitVar	rs201672011
Map	rs201672011
PheGenI	rs201672011
Biobank	rs201672011
1000 genomes	rs201672011
hgdp	rs201672011
ensembl	rs201672011
geneview	rs201672011
scholar	rs201672011
google	rs201672011
pharmgkb	rs201672011
gwascentral	rs201672011
openSNP	rs201672011
23andMe	rs201672011
SNPshot	rs201672011
SNPdbe	rs201672011
MSV3d	rs201672011
GWAS Ctlg	rs201672011

GMAF

0.0004591

Max Magnitude

0

ClinVar
Risk	rs201672011(A;A)
Alt	rs201672011(A;A)
Reference	Rs201672011(G;G)
Significance	Pathogenic
Disease	Familial type 3 hyperlipoproteinemia Hypercholesterolemia and hypertriglyceridemia
Variation	info
Gene	APOE
CLNDBN	Familial type 3 hyperlipoproteinemia Hypercholesterolemia and hypertriglyceridemia, type III
Reversed	0
HGVS	NC_000019.9:g.45411064G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019443.28, RCV000019453.28,