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rs374603772

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs374603772(C;T)
Make rs374603772(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position55058630
GenePCSK9
is asnp
is mentioned by
dbSNPrs374603772
ebirs374603772
HLIrs374603772
Exacrs374603772
Varsomers374603772
Maprs374603772
PheGenIrs374603772
hapmaprs374603772
1000 genomesrs374603772
hgdprs374603772
ensemblrs374603772
gopubmedrs374603772
geneviewrs374603772
scholarrs374603772
googlers374603772
pharmgkbrs374603772
gwascentralrs374603772
openSNPrs374603772
23andMers374603772
23andMe allrs374603772
SNP Nexus

SNPshotrs374603772
SNPdbers374603772
MSV3drs374603772
GWAS Ctlgrs374603772
Max Magnitude0
ClinVar
Risk rs374603772(T;T)
Alt rs374603772(T;T)
Reference rs374603772(C;C)
Significance Pathogenic
Disease not provided Hypercholesterolemia
Variation info
Gene PCSK9
CLNDBN not provided Hypercholesterolemia, autosomal dominant, 3
Reversed 0
HGVS NC_000001.10:g.55524303C>T
CLNSRC
CLNACC RCV000182577.1, RCV000231738.1,