rs1529927
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs1529927(C;C) |
Make rs1529927(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 56870675 |
Gene | SLC12A3 |
is a | snp |
is | mentioned by |
dbSNP | rs1529927 |
dbSNP (classic) | rs1529927 |
ClinGen | rs1529927 |
ebi | rs1529927 |
HLI | rs1529927 |
Exac | rs1529927 |
Gnomad | rs1529927 |
Varsome | rs1529927 |
LitVar | rs1529927 |
Map | rs1529927 |
PheGenI | rs1529927 |
Biobank | rs1529927 |
1000 genomes | rs1529927 |
hgdp | rs1529927 |
ensembl | rs1529927 |
geneview | rs1529927 |
scholar | rs1529927 |
rs1529927 | |
pharmgkb | rs1529927 |
gwascentral | rs1529927 |
openSNP | rs1529927 |
23andMe | rs1529927 |
SNPshot | rs1529927 |
SNPdbe | rs1529927 |
MSV3d | rs1529927 |
GWAS Ctlg | rs1529927 |
GMAF | 0.01791 |
Max Magnitude | 0 |
This SNP is cited in US patent 10,465,246 (2019), where one of the claims is prescribing a hydrochlorothiazide to a patient as a first line therapy (for high blood pressure), without a beta blocker and without a vasodilator, if the patient carries a rs1529927(T). Note that this appears to be an error in the patent as written and as issued; the authors likely should have written rs1529927(C).
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|