rs1230399
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1230399(C;C) |
Make rs1230399(C;T) |
Make rs1230399(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 43768035 |
Gene | DUSP3 |
is a | snp |
is | mentioned by |
dbSNP | rs1230399 |
dbSNP (classic) | rs1230399 |
ClinGen | rs1230399 |
ebi | rs1230399 |
HLI | rs1230399 |
Exac | rs1230399 |
Gnomad | rs1230399 |
Varsome | rs1230399 |
LitVar | rs1230399 |
Map | rs1230399 |
PheGenI | rs1230399 |
Biobank | rs1230399 |
1000 genomes | rs1230399 |
hgdp | rs1230399 |
ensembl | rs1230399 |
geneview | rs1230399 |
scholar | rs1230399 |
rs1230399 | |
pharmgkb | rs1230399 |
gwascentral | rs1230399 |
openSNP | rs1230399 |
23andMe | rs1230399 |
SNPshot | rs1230399 |
SNPdbe | rs1230399 |
MSV3d | rs1230399 |
GWAS Ctlg | rs1230399 |
GMAF | 0.2938 |
Max Magnitude | 0 |
[PMID 19371798] The -9247 T/C polymorphism in the SOST upstream regulatory region that potentially affects C/EBPalpha and FOXA1 binding is associated with osteoporosis