rs267606663

Orientation

plus

Stabilized

plus

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

Make rs267606663(A;A)

Make rs267606663(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

44909021

Gene

APOE

is a	snp
is	mentioned by
dbSNP	rs267606663
dbSNP (classic)	rs267606663
ClinGen	rs267606663
ebi	rs267606663
HLI	rs267606663
Exac	rs267606663
Gnomad	rs267606663
Varsome	rs267606663
LitVar	rs267606663
Map	rs267606663
PheGenI	rs267606663
Biobank	rs267606663
1000 genomes	rs267606663
hgdp	rs267606663
ensembl	rs267606663
geneview	rs267606663
scholar	rs267606663
google	rs267606663
pharmgkb	rs267606663
gwascentral	rs267606663
openSNP	rs267606663
23andMe	rs267606663
SNPshot	rs267606663
SNPdbe	rs267606663
MSV3d	rs267606663
GWAS Ctlg	rs267606663

Max Magnitude

0

ClinVar
Risk	rs267606663(A;A) rs267606663(C;C)
Alt	rs267606663(A;A) rs267606663(C;C)
Reference	Rs267606663(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.45412278G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019452.30,