rs562574661

Orientation

plus

Stabilized

plus

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

Make rs562574661(-;-)

Make rs562574661(-;CTG)

Reference

GRCh38.p7 38.3/149

Chromosome

2

Position

21001940

Gene

APOB

is a	snp
is	mentioned by
dbSNP	rs562574661
dbSNP (classic)	rs562574661
ClinGen	rs562574661
ebi	rs562574661
HLI	rs562574661
Exac	rs562574661
Gnomad	rs562574661
Varsome	rs562574661
LitVar	rs562574661
Map	rs562574661
PheGenI	rs562574661
Biobank	rs562574661
1000 genomes	rs562574661
hgdp	rs562574661
ensembl	rs562574661
geneview	rs562574661
scholar	rs562574661
google	rs562574661
pharmgkb	rs562574661
gwascentral	rs562574661
openSNP	rs562574661
23andMe	rs562574661
SNPshot	rs562574661
SNPdbe	rs562574661
MSV3d	rs562574661
GWAS Ctlg	rs562574661

Max Magnitude

0

ClinVar
Risk	rs562574661(-;-)
Alt	rs562574661(-;-)
Reference	Rs562574661(CTG;CTG)
Significance	Other
Disease	Familial hypercholesterolemia
Variation	info
Gene	APOB
CLNDBN	Familial hypercholesterolemia
Reversed	0
HGVS	NC_000002.11:g.21224812_21224814delCTG
CLNSRC	Instituto Nacional de Saúde Doutor Ricardo Jorge The University of Western Ontario
CLNACC	RCV000256307.1,