rs542881762
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs542881762(C;T) |
Make rs542881762(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 173907528 |
Gene | SERPINC1 |
is a | snp |
is | mentioned by |
dbSNP | rs542881762 |
dbSNP (classic) | rs542881762 |
ClinGen | rs542881762 |
ebi | rs542881762 |
HLI | rs542881762 |
Exac | rs542881762 |
Gnomad | rs542881762 |
Varsome | rs542881762 |
LitVar | rs542881762 |
Map | rs542881762 |
PheGenI | rs542881762 |
Biobank | rs542881762 |
1000 genomes | rs542881762 |
hgdp | rs542881762 |
ensembl | rs542881762 |
geneview | rs542881762 |
scholar | rs542881762 |
rs542881762 | |
pharmgkb | rs542881762 |
gwascentral | rs542881762 |
openSNP | rs542881762 |
23andMe | rs542881762 |
SNPshot | rs542881762 |
SNPdbe | rs542881762 |
MSV3d | rs542881762 |
GWAS Ctlg | rs542881762 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs542881762(G;G) rs542881762(T;T) |
Alt | rs542881762(G;G) rs542881762(T;T) |
Reference | Rs542881762(C;C) |
Significance | Probable-Pathogenic |
Disease | Antithrombin III deficiency |
Variation | info |
Gene | SERPINC1 |
CLNDBN | Antithrombin III deficiency |
Reversed | 0 |
HGVS | NC_000001.10:g.173876666C>T |
CLNSRC | |
CLNACC | RCV000456535.1, |