rs778738291

Orientation

plus

Stabilized

plus

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

Make rs778738291(A;A)

Make rs778738291(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

55044020

Gene

PCSK9

is a	snp
is	mentioned by
dbSNP	rs778738291
dbSNP (classic)	rs778738291
ClinGen	rs778738291
ebi	rs778738291
HLI	rs778738291
Exac	rs778738291
Gnomad	rs778738291
Varsome	rs778738291
LitVar	rs778738291
Map	rs778738291
PheGenI	rs778738291
Biobank	rs778738291
1000 genomes	rs778738291
hgdp	rs778738291
ensembl	rs778738291
geneview	rs778738291
scholar	rs778738291
google	rs778738291
pharmgkb	rs778738291
gwascentral	rs778738291
openSNP	rs778738291
23andMe	rs778738291
SNPshot	rs778738291
SNPdbe	rs778738291
MSV3d	rs778738291
GWAS Ctlg	rs778738291

Max Magnitude

0

ClinVar
Risk	rs778738291(A;A)
Alt	rs778738291(A;A)
Reference	Rs778738291(G;G)
Significance	Probable-Pathogenic
Disease	Hypercholesterolemia
Variation	info
Gene	PCSK9
CLNDBN	Hypercholesterolemia, autosomal dominant, 3
Reversed	0
HGVS	NC_000001.10:g.55509693G>A
CLNSRC
CLNACC	RCV000417258.1,