rs7855483
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7855483(C;C) |
Make rs7855483(C;T) |
Make rs7855483(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 32372464 |
is a | snp |
is | mentioned by |
dbSNP | rs7855483 |
dbSNP (classic) | rs7855483 |
ClinGen | rs7855483 |
ebi | rs7855483 |
HLI | rs7855483 |
Exac | rs7855483 |
Gnomad | rs7855483 |
Varsome | rs7855483 |
LitVar | rs7855483 |
Map | rs7855483 |
PheGenI | rs7855483 |
Biobank | rs7855483 |
1000 genomes | rs7855483 |
hgdp | rs7855483 |
ensembl | rs7855483 |
geneview | rs7855483 |
scholar | rs7855483 |
rs7855483 | |
pharmgkb | rs7855483 |
gwascentral | rs7855483 |
openSNP | rs7855483 |
23andMe | rs7855483 |
SNPshot | rs7855483 |
SNPdbe | rs7855483 |
MSV3d | rs7855483 |
GWAS Ctlg | rs7855483 |
GMAF | 0.2406 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20574843] Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations