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rs772677312

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs772677312(C;G)
Make rs772677312(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position55058543
GenePCSK9
is asnp
is mentioned by
dbSNPrs772677312
dbSNP (classic)rs772677312
ClinGenrs772677312
ebirs772677312
HLIrs772677312
Exacrs772677312
Gnomadrs772677312
Varsomers772677312
LitVarrs772677312
Maprs772677312
PheGenIrs772677312
Biobankrs772677312
1000 genomesrs772677312
hgdprs772677312
ensemblrs772677312
geneviewrs772677312
scholarrs772677312
googlers772677312
pharmgkbrs772677312
gwascentralrs772677312
openSNPrs772677312
23andMers772677312
SNPshotrs772677312
SNPdbers772677312
MSV3drs772677312
GWAS Ctlgrs772677312
Max Magnitude0
ClinVar
Risk rs772677312(G;G)
Alt rs772677312(G;G)
Reference Rs772677312(C;C)
Significance Other
Disease Familial hypercholesterolemia
Variation info
Gene PCSK9
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000001.10:g.55524216C>G
CLNSRC Instituto Nacional de Saúde Doutor Ricardo Jorge
CLNACC RCV000256342.1,