rs17288067
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 |
Make rs17288067(A;A) |
Make rs17288067(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 32409048 |
Gene | ACO1 |
is a | snp |
is | mentioned by |
dbSNP | rs17288067 |
dbSNP (classic) | rs17288067 |
ClinGen | rs17288067 |
ebi | rs17288067 |
HLI | rs17288067 |
Exac | rs17288067 |
Gnomad | rs17288067 |
Varsome | rs17288067 |
LitVar | rs17288067 |
Map | rs17288067 |
PheGenI | rs17288067 |
Biobank | rs17288067 |
1000 genomes | rs17288067 |
hgdp | rs17288067 |
ensembl | rs17288067 |
geneview | rs17288067 |
scholar | rs17288067 |
rs17288067 | |
pharmgkb | rs17288067 |
gwascentral | rs17288067 |
openSNP | rs17288067 |
23andMe | rs17288067 |
SNPshot | rs17288067 |
SNPdbe | rs17288067 |
MSV3d | rs17288067 |
GWAS Ctlg | rs17288067 |
GMAF | 0.1139 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20574843] Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations