rs28931578

Orientation

plus

Stabilized

plus

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

Make rs28931578(A;A)

Make rs28931578(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

44908751

Gene

APOE

is a	snp
is	mentioned by
dbSNP	rs28931578
dbSNP (classic)	rs28931578
ClinGen	rs28931578
ebi	rs28931578
HLI	rs28931578
Exac	rs28931578
Gnomad	rs28931578
Varsome	rs28931578
LitVar	rs28931578
Map	rs28931578
PheGenI	rs28931578
Biobank	rs28931578
1000 genomes	rs28931578
hgdp	rs28931578
ensembl	rs28931578
geneview	rs28931578
scholar	rs28931578
google	rs28931578
pharmgkb	rs28931578
gwascentral	rs28931578
openSNP	rs28931578
23andMe	rs28931578
SNPshot	rs28931578
SNPdbe	rs28931578
MSV3d	rs28931578
GWAS Ctlg	rs28931578

Max Magnitude

0

OMIM	107741
Desc	APOE2 VARIANT
Variant	0027
Related	also

ClinVar
Risk	rs28931578(A;A) rs28931578(C;C)
Alt	rs28931578(A;A) rs28931578(C;C)
Reference	Rs28931578(G;G)
Significance	Pathogenic
Disease	APOE2 VARIANT
Variation	info
Gene	APOE
CLNDBN	APOE2 VARIANT
Reversed	0
HGVS	NC_000019.9:g.45412008G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019460.28,