rs369067856
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs369067856(C;C) |
Make rs369067856(C;T) |
Make rs369067856(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 55043945 |
Gene | PCSK9 |
is a | snp |
is | mentioned by |
dbSNP | rs369067856 |
dbSNP (classic) | rs369067856 |
ClinGen | rs369067856 |
ebi | rs369067856 |
HLI | rs369067856 |
Exac | rs369067856 |
Gnomad | rs369067856 |
Varsome | rs369067856 |
LitVar | rs369067856 |
Map | rs369067856 |
PheGenI | rs369067856 |
Biobank | rs369067856 |
1000 genomes | rs369067856 |
hgdp | rs369067856 |
ensembl | rs369067856 |
geneview | rs369067856 |
scholar | rs369067856 |
rs369067856 | |
pharmgkb | rs369067856 |
gwascentral | rs369067856 |
openSNP | rs369067856 |
23andMe | rs369067856 |
SNPshot | rs369067856 |
SNPdbe | rs369067856 |
MSV3d | rs369067856 |
GWAS Ctlg | rs369067856 |
Max Magnitude | 0 |
PCSK9 mutation; possible association with diabetes, according to [PMID 19762784]