rs11083750

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs11083750(C;G)

Make rs11083750(G;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

44908601

Gene

APOE

is a	snp
is	mentioned by
dbSNP	rs11083750
dbSNP (classic)	rs11083750
ClinGen	rs11083750
ebi	rs11083750
HLI	rs11083750
Exac	rs11083750
Gnomad	rs11083750
Varsome	rs11083750
LitVar	rs11083750
Map	rs11083750
PheGenI	rs11083750
Biobank	rs11083750
1000 genomes	rs11083750
hgdp	rs11083750
ensembl	rs11083750
geneview	rs11083750
scholar	rs11083750
google	rs11083750
pharmgkb	rs11083750
gwascentral	rs11083750
openSNP	rs11083750
23andMe	rs11083750
SNPshot	rs11083750
SNPdbe	rs11083750
MSV3d	rs11083750
GWAS Ctlg	rs11083750

Max Magnitude

0

OMIM	107741
Desc	APOE4 VARIANT
Variant	0025
Related	also

ClinVar
Risk	rs11083750(A;A) rs11083750(G;G) rs11083750(T;T)
Alt	rs11083750(A;A) rs11083750(G;G) rs11083750(T;T)
Reference	Rs11083750(C;C)
Significance	Other
Disease	APOE4 VARIANT
Variation	info
Gene	APOE
CLNDBN	APOE4 VARIANT
Reversed	0
HGVS	NC_000019.9:g.45411858C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019458.24,