rs17179670
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17179670(A;A) |
Make rs17179670(A;G) |
Make rs17179670(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 65956032 |
Gene | HMGA2 |
is a | snp |
is | mentioned by |
dbSNP | rs17179670 |
dbSNP (classic) | rs17179670 |
ClinGen | rs17179670 |
ebi | rs17179670 |
HLI | rs17179670 |
Exac | rs17179670 |
Gnomad | rs17179670 |
Varsome | rs17179670 |
LitVar | rs17179670 |
Map | rs17179670 |
PheGenI | rs17179670 |
Biobank | rs17179670 |
1000 genomes | rs17179670 |
hgdp | rs17179670 |
ensembl | rs17179670 |
geneview | rs17179670 |
scholar | rs17179670 |
rs17179670 | |
pharmgkb | rs17179670 |
gwascentral | rs17179670 |
openSNP | rs17179670 |
23andMe | rs17179670 |
SNPshot | rs17179670 |
SNPdbe | rs17179670 |
MSV3d | rs17179670 |
GWAS Ctlg | rs17179670 |
GMAF | 0.1309 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
Rs17179670 is a SNP implicated in Tooth Development
[PMID 21358824] Prostate cancer susceptibility Loci identified on chromosome 12 in African Americans.