rs979976
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs979976(A;A) |
Make rs979976(A;C) |
Make rs979976(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 137011132 |
Gene | THSD7B |
is a | snp |
is | mentioned by |
dbSNP | rs979976 |
dbSNP (classic) | rs979976 |
ClinGen | rs979976 |
ebi | rs979976 |
HLI | rs979976 |
Exac | rs979976 |
Gnomad | rs979976 |
Varsome | rs979976 |
LitVar | rs979976 |
Map | rs979976 |
PheGenI | rs979976 |
Biobank | rs979976 |
1000 genomes | rs979976 |
hgdp | rs979976 |
ensembl | rs979976 |
geneview | rs979976 |
scholar | rs979976 |
rs979976 | |
pharmgkb | rs979976 |
gwascentral | rs979976 |
openSNP | rs979976 |
23andMe | rs979976 |
SNPshot | rs979976 |
SNPdbe | rs979976 |
MSV3d | rs979976 |
GWAS Ctlg | rs979976 |
GMAF | 0.3944 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23761726] |
Trait | Corneal astigmatism |
Title | Interrogation of the platelet-derived growth factor receptor alpha locus and corneal astigmatism in Australians of Northern European ancestry: Results of a genome-wide association study. |
Risk Allele | A |
P-val | 8E-6 |
Odds Ratio | .13 [0.075-0.193] unit increase |