Have questions? Visit https://www.reddit.com/r/SNPedia

rs793888521

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs793888521(A;A)
Make rs793888521(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position55052364
GenePCSK9
is asnp
is mentioned by
dbSNPrs793888521
ebirs793888521
HLIrs793888521
Exacrs793888521
Varsomers793888521
Maprs793888521
PheGenIrs793888521
hapmaprs793888521
1000 genomesrs793888521
hgdprs793888521
ensemblrs793888521
gopubmedrs793888521
geneviewrs793888521
scholarrs793888521
googlers793888521
pharmgkbrs793888521
gwascentralrs793888521
openSNPrs793888521
23andMers793888521
23andMe allrs793888521
SNP Nexus

SNPshotrs793888521
SNPdbers793888521
MSV3drs793888521
GWAS Ctlgrs793888521
Max Magnitude0
ClinVar
Risk rs793888521(A;A)
Alt rs793888521(A;A)
Reference rs793888521(G;G)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene PCSK9
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000001.10:g.55518037G>A
CLNSRC
CLNACC RCV000172975.1,