rs1051929
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1051929(A;A) |
Make rs1051929(A;G) |
Make rs1051929(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 176172026 |
Gene | HOXD3 |
is a | snp |
is | mentioned by |
dbSNP | rs1051929 |
dbSNP (classic) | rs1051929 |
ClinGen | rs1051929 |
ebi | rs1051929 |
HLI | rs1051929 |
Exac | rs1051929 |
Gnomad | rs1051929 |
Varsome | rs1051929 |
LitVar | rs1051929 |
Map | rs1051929 |
PheGenI | rs1051929 |
Biobank | rs1051929 |
1000 genomes | rs1051929 |
hgdp | rs1051929 |
ensembl | rs1051929 |
geneview | rs1051929 |
scholar | rs1051929 |
rs1051929 | |
pharmgkb | rs1051929 |
gwascentral | rs1051929 |
openSNP | rs1051929 |
23andMe | rs1051929 |
SNPshot | rs1051929 |
SNPdbe | rs1051929 |
MSV3d | rs1051929 |
GWAS Ctlg | rs1051929 |
GMAF | 0.236 |
Max Magnitude | 0 |
[PMID 24127533] The absence of mutations in homeobox candidate genes HOXA3, HOXB3, HOXD3 and PITX2 in familial and sporadic thyroid hemiagenesis