rs121918397

Orientation

plus

Stabilized

plus

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

Make rs121918397(A;A)

Make rs121918397(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

44908784

Gene

APOE

is a	snp
is	mentioned by
dbSNP	rs121918397
dbSNP (classic)	rs121918397
ClinGen	rs121918397
ebi	rs121918397
HLI	rs121918397
Exac	rs121918397
Gnomad	rs121918397
Varsome	rs121918397
LitVar	rs121918397
Map	rs121918397
PheGenI	rs121918397
Biobank	rs121918397
1000 genomes	rs121918397
hgdp	rs121918397
ensembl	rs121918397
geneview	rs121918397
scholar	rs121918397
google	rs121918397
pharmgkb	rs121918397
gwascentral	rs121918397
openSNP	rs121918397
23andMe	rs121918397
SNPshot	rs121918397
SNPdbe	rs121918397
MSV3d	rs121918397
GWAS Ctlg	rs121918397

Max Magnitude

0

OMIM	107741
Desc
Variant	0018
Related	also

OMIM	107741
Desc
Variant	0032
Related	also

ClinVar
Risk	rs121918397(A;A) rs121918397(C;C)
Alt	rs121918397(A;A) rs121918397(C;C)
Reference	Rs121918397(G;G)
Significance	Pathogenic
Disease	Familial type 3 hyperlipoproteinemia Lipoprotein glomerulopathy
Variation	info
Gene	APOE
CLNDBN	Familial type 3 hyperlipoproteinemia Lipoprotein glomerulopathy
Reversed	0
HGVS	NC_000019.9:g.45412041G>A; NC_000019.9:g.45412041G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019449.29, RCV000019466.24,