rs28931579

Orientation

plus

Stabilized

plus

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

Make rs28931579(A;C)

Make rs28931579(C;C)

Reference

GRCh38 38.1/141

Chromosome

19

Position

44909236

Gene

APOE

is a	snp
is	mentioned by
dbSNP	rs28931579
dbSNP (classic)	rs28931579
ClinGen	rs28931579
ebi	rs28931579
HLI	rs28931579
Exac	rs28931579
Gnomad	rs28931579
Varsome	rs28931579
LitVar	rs28931579
Map	rs28931579
PheGenI	rs28931579
Biobank	rs28931579
1000 genomes	rs28931579
hgdp	rs28931579
ensembl	rs28931579
geneview	rs28931579
scholar	rs28931579
google	rs28931579
pharmgkb	rs28931579
gwascentral	rs28931579
openSNP	rs28931579
23andMe	rs28931579
SNPshot	rs28931579
SNPdbe	rs28931579
MSV3d	rs28931579
GWAS Ctlg	rs28931579

Max Magnitude

0

OMIM	107741
Desc	APOE4(+)
Variant	0029
Related	also

ClinVar
Risk	rs28931579(C;C)
Alt	rs28931579(C;C)
Reference	Rs28931579(A;A)
Significance	Pathogenic
Disease	APOE4(+)
Variation	info
Gene	APOE
CLNDBN	APOE4(+)
Reversed	0
HGVS	NC_000019.9:g.45412493A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019462.28,