rs190853081

Orientation

plus

Stabilized

plus

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

Make rs190853081(A;A)

Make rs190853081(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

44909083

Gene

APOE

is a	snp
is	mentioned by
dbSNP	rs190853081
dbSNP (classic)	rs190853081
ClinGen	rs190853081
ebi	rs190853081
HLI	rs190853081
Exac	rs190853081
Gnomad	rs190853081
Varsome	rs190853081
LitVar	rs190853081
Map	rs190853081
PheGenI	rs190853081
Biobank	rs190853081
1000 genomes	rs190853081
hgdp	rs190853081
ensembl	rs190853081
geneview	rs190853081
scholar	rs190853081
google	rs190853081
pharmgkb	rs190853081
gwascentral	rs190853081
openSNP	rs190853081
23andMe	rs190853081
SNPshot	rs190853081
SNPdbe	rs190853081
MSV3d	rs190853081
GWAS Ctlg	rs190853081

GMAF

0.0009183

Max Magnitude

0

ClinVar
Risk	rs190853081(A;A)
Alt	rs190853081(A;A)
Reference	Rs190853081(G;G)
Significance	Pathogenic
Disease	Familial type 3 hyperlipoproteinemia
Variation	info
Gene	APOE
CLNDBN	Familial type 3 hyperlipoproteinemia
Reversed	0
HGVS	NC_000019.9:g.45412340G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019435.30,