rs587777759
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs587777759(-;T) |
Make rs587777759(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 22 |
Position | 20779633 |
Gene | PI4KA, SERPIND1 |
is a | snp |
is | mentioned by |
dbSNP | rs587777759 |
dbSNP (classic) | rs587777759 |
ClinGen | rs587777759 |
ebi | rs587777759 |
HLI | rs587777759 |
Exac | rs587777759 |
Gnomad | rs587777759 |
Varsome | rs587777759 |
LitVar | rs587777759 |
Map | rs587777759 |
PheGenI | rs587777759 |
Biobank | rs587777759 |
1000 genomes | rs587777759 |
hgdp | rs587777759 |
ensembl | rs587777759 |
geneview | rs587777759 |
scholar | rs587777759 |
rs587777759 | |
pharmgkb | rs587777759 |
gwascentral | rs587777759 |
openSNP | rs587777759 |
23andMe | rs587777759 |
SNPshot | rs587777759 |
SNPdbe | rs587777759 |
MSV3d | rs587777759 |
GWAS Ctlg | rs587777759 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587777759(T;T) |
Alt | rs587777759(T;T) |
Reference | Rs587777759(-;-) |
Significance | Pathogenic |
Disease | Heparin cofactor II deficiency |
Variation | info |
Gene | SERPIND1 PI4KA |
CLNDBN | Heparin cofactor II deficiency |
Reversed | 0 |
HGVS | NC_000022.10:g.21133921dupT |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000016093.26, |