rs121918396

Orientation

plus

Stabilized

plus

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

Make rs121918396(A;A)

Make rs121918396(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

44908979

Gene

APOE

is a	snp
is	mentioned by
dbSNP	rs121918396
dbSNP (classic)	rs121918396
ClinGen	rs121918396
ebi	rs121918396
HLI	rs121918396
Exac	rs121918396
Gnomad	rs121918396
Varsome	rs121918396
LitVar	rs121918396
Map	rs121918396
PheGenI	rs121918396
Biobank	rs121918396
1000 genomes	rs121918396
hgdp	rs121918396
ensembl	rs121918396
geneview	rs121918396
scholar	rs121918396
google	rs121918396
pharmgkb	rs121918396
gwascentral	rs121918396
openSNP	rs121918396
23andMe	rs121918396
SNPshot	rs121918396
SNPdbe	rs121918396
MSV3d	rs121918396
GWAS Ctlg	rs121918396

Max Magnitude

0

OMIM	107741
Desc
Variant	0014
Related	also

ClinVar
Risk	rs121918396(A;A)
Alt	rs121918396(A;A)
Reference	Rs121918396(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.45412236G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019445.24,