rs267606661

Orientation

plus

Stabilized

plus

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

Make rs267606661(C;G)

Make rs267606661(G;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

44909101

Gene

APOE

is a	snp
is	mentioned by
dbSNP	rs267606661
dbSNP (classic)	rs267606661
ClinGen	rs267606661
ebi	rs267606661
HLI	rs267606661
Exac	rs267606661
Gnomad	rs267606661
Varsome	rs267606661
LitVar	rs267606661
Map	rs267606661
PheGenI	rs267606661
Biobank	rs267606661
1000 genomes	rs267606661
hgdp	rs267606661
ensembl	rs267606661
geneview	rs267606661
scholar	rs267606661
google	rs267606661
pharmgkb	rs267606661
gwascentral	rs267606661
openSNP	rs267606661
23andMe	rs267606661
SNPshot	rs267606661
SNPdbe	rs267606661
MSV3d	rs267606661
GWAS Ctlg	rs267606661

Max Magnitude

0

ClinVar
Risk	rs267606661(G;G) rs267606661(T;T)
Alt	rs267606661(G;G) rs267606661(T;T)
Reference	Rs267606661(C;C)
Significance	Pathogenic
Disease	Familial type 3 hyperlipoproteinemia
Variation	info
Gene	APOE
CLNDBN	Familial type 3 hyperlipoproteinemia
Reversed	0
HGVS	NC_000019.9:g.45412358C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019455.29,