rs1057516136

Orientation

plus

Stabilized

plus

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

Make rs1057516136(A;G)

Make rs1057516136(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

55059519

Gene

PCSK9

is a	snp
is	mentioned by
dbSNP	rs1057516136
dbSNP (classic)	rs1057516136
ClinGen	rs1057516136
ebi	rs1057516136
HLI	rs1057516136
Exac	rs1057516136
Gnomad	rs1057516136
Varsome	rs1057516136
LitVar	rs1057516136
Map	rs1057516136
PheGenI	rs1057516136
Biobank	rs1057516136
1000 genomes	rs1057516136
hgdp	rs1057516136
ensembl	rs1057516136
geneview	rs1057516136
scholar	rs1057516136
google	rs1057516136
pharmgkb	rs1057516136
gwascentral	rs1057516136
openSNP	rs1057516136
23andMe	rs1057516136
SNPshot	rs1057516136
SNPdbe	rs1057516136
MSV3d	rs1057516136
GWAS Ctlg	rs1057516136

Max Magnitude

0

ClinVar
Risk	rs1057516136(G;G)
Alt	rs1057516136(G;G)
Reference	Rs1057516136(A;A)
Significance	Probable-Pathogenic
Disease	Familial hypercholesterolemia
Variation	info
Gene	PCSK9
CLNDBN	Familial hypercholesterolemia
Reversed	0
HGVS	NC_000001.10:g.55525192A>G
CLNSRC
CLNACC	RCV000408784.1,