rs3024778
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs3024778(A;A) |
Make rs3024778(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 113160151 |
Gene | PROZ |
is a | snp |
is | mentioned by |
dbSNP | rs3024778 |
dbSNP (classic) | rs3024778 |
ClinGen | rs3024778 |
ebi | rs3024778 |
HLI | rs3024778 |
Exac | rs3024778 |
Gnomad | rs3024778 |
Varsome | rs3024778 |
LitVar | rs3024778 |
Map | rs3024778 |
PheGenI | rs3024778 |
Biobank | rs3024778 |
1000 genomes | rs3024778 |
hgdp | rs3024778 |
ensembl | rs3024778 |
geneview | rs3024778 |
scholar | rs3024778 |
rs3024778 | |
pharmgkb | rs3024778 |
gwascentral | rs3024778 |
openSNP | rs3024778 |
23andMe | rs3024778 |
SNPshot | rs3024778 |
SNPdbe | rs3024778 |
MSV3d | rs3024778 |
GWAS Ctlg | rs3024778 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19050305] Association of the protein Z ATG haplotype with symptomatic nonvascular stroke or thromboembolism in white children: a family-based cohort study
[PMID 23420821] Protein Z variants associated with protein Z plasma levels and with risk of idiopathic recurrent miscarriage.