rs10453441
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10453441(A;A) |
Make rs10453441(A;G) |
Make rs10453441(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 22 |
Position | 45967859 |
Gene | WNT7B |
is a | snp |
is | mentioned by |
dbSNP | rs10453441 |
dbSNP (classic) | rs10453441 |
ClinGen | rs10453441 |
ebi | rs10453441 |
HLI | rs10453441 |
Exac | rs10453441 |
Gnomad | rs10453441 |
Varsome | rs10453441 |
LitVar | rs10453441 |
Map | rs10453441 |
PheGenI | rs10453441 |
Biobank | rs10453441 |
1000 genomes | rs10453441 |
hgdp | rs10453441 |
ensembl | rs10453441 |
geneview | rs10453441 |
scholar | rs10453441 |
rs10453441 | |
pharmgkb | rs10453441 |
gwascentral | rs10453441 |
openSNP | rs10453441 |
23andMe | rs10453441 |
SNPshot | rs10453441 |
SNPdbe | rs10453441 |
MSV3d | rs10453441 |
GWAS Ctlg | rs10453441 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 27655401] Genome-Wide Association Study Identifies WNT7B as a Novel Locus for Central Corneal Thickness in Latinos.
[PMID 29847655] Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus.