rs34729309
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs34729309(A;A) |
Make rs34729309(A;C) |
Make rs34729309(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 2 |
Position | 176169393 |
Gene | HOXD3 |
is a | snp |
is | mentioned by |
dbSNP | rs34729309 |
dbSNP (classic) | rs34729309 |
ClinGen | rs34729309 |
ebi | rs34729309 |
HLI | rs34729309 |
Exac | rs34729309 |
Gnomad | rs34729309 |
Varsome | rs34729309 |
LitVar | rs34729309 |
Map | rs34729309 |
PheGenI | rs34729309 |
Biobank | rs34729309 |
1000 genomes | rs34729309 |
hgdp | rs34729309 |
ensembl | rs34729309 |
geneview | rs34729309 |
scholar | rs34729309 |
rs34729309 | |
pharmgkb | rs34729309 |
gwascentral | rs34729309 |
openSNP | rs34729309 |
23andMe | rs34729309 |
SNPshot | rs34729309 |
SNPdbe | rs34729309 |
MSV3d | rs34729309 |
GWAS Ctlg | rs34729309 |
GMAF | 0.1938 |
Max Magnitude | 0 |
[PMID 24127533] The absence of mutations in homeobox candidate genes HOXA3, HOXB3, HOXD3 and PITX2 in familial and sporadic thyroid hemiagenesis