rs374603772

Orientation

plus

Stabilized

plus

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

Make rs374603772(C;T)

Make rs374603772(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

55058630

Gene

PCSK9

is a	snp
is	mentioned by
dbSNP	rs374603772
dbSNP (classic)	rs374603772
ClinGen	rs374603772
ebi	rs374603772
HLI	rs374603772
Exac	rs374603772
Gnomad	rs374603772
Varsome	rs374603772
LitVar	rs374603772
Map	rs374603772
PheGenI	rs374603772
Biobank	rs374603772
1000 genomes	rs374603772
hgdp	rs374603772
ensembl	rs374603772
geneview	rs374603772
scholar	rs374603772
google	rs374603772
pharmgkb	rs374603772
gwascentral	rs374603772
openSNP	rs374603772
23andMe	rs374603772
SNPshot	rs374603772
SNPdbe	rs374603772
MSV3d	rs374603772
GWAS Ctlg	rs374603772

Max Magnitude

0

ClinVar
Risk	rs374603772(T;T)
Alt	rs374603772(T;T)
Reference	Rs374603772(C;C)
Significance	Other
Disease	Hypercholesterolemia not specified
Variation	info
Gene	PCSK9
CLNDBN	Hypercholesterolemia, autosomal dominant, 3 not specified
Reversed	0
HGVS	NC_000001.10:g.55524303C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000231738.2, RCV000455706.1,