rs267606662

Orientation

plus

Stabilized

plus

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

Make rs267606662(C;C)

Make rs267606662(C;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

44908804

Gene

APOE

is a	snp
is	mentioned by
dbSNP	rs267606662
dbSNP (classic)	rs267606662
ClinGen	rs267606662
ebi	rs267606662
HLI	rs267606662
Exac	rs267606662
Gnomad	rs267606662
Varsome	rs267606662
LitVar	rs267606662
Map	rs267606662
PheGenI	rs267606662
Biobank	rs267606662
1000 genomes	rs267606662
hgdp	rs267606662
ensembl	rs267606662
geneview	rs267606662
scholar	rs267606662
google	rs267606662
pharmgkb	rs267606662
gwascentral	rs267606662
openSNP	rs267606662
23andMe	rs267606662
SNPshot	rs267606662
SNPdbe	rs267606662
MSV3d	rs267606662
GWAS Ctlg	rs267606662

Max Magnitude

0

ClinVar
Risk	rs267606662(C;C)
Alt	rs267606662(C;C)
Reference	Rs267606662(G;G)
Significance	Pathogenic
Disease	APOE3 VARIANT
Variation	info
Gene	APOE
CLNDBN	APOE3 VARIANT
Reversed	0
HGVS	NC_000019.9:g.45412061G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019459.28,