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rs778849441

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs778849441(C;T)
Make rs778849441(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position55058538
GenePCSK9
is asnp
is mentioned by
dbSNPrs778849441
dbSNP (classic)rs778849441
ClinGenrs778849441
ebirs778849441
HLIrs778849441
Exacrs778849441
Gnomadrs778849441
Varsomers778849441
LitVarrs778849441
Maprs778849441
PheGenIrs778849441
Biobankrs778849441
1000 genomesrs778849441
hgdprs778849441
ensemblrs778849441
geneviewrs778849441
scholarrs778849441
googlers778849441
pharmgkbrs778849441
gwascentralrs778849441
openSNPrs778849441
23andMers778849441
23andMe allrs778849441
SNPshotrs778849441
SNPdbers778849441
MSV3drs778849441
GWAS Ctlgrs778849441
Max Magnitude0
ClinVar
Risk rs778849441(G;G) rs778849441(T;T)
Alt rs778849441(G;G) rs778849441(T;T)
Reference Rs778849441(C;C)
Significance Probable-Pathogenic
Disease not specified Hypercholesterolemia
Variation info
Gene PCSK9
CLNDBN not specified Hypercholesterolemia, autosomal dominant, 3
Reversed 0
HGVS NC_000001.10:g.55524211C>T
CLNSRC
CLNACC RCV000454751.1, RCV000460891.1,