rs17204952
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17204952(C;C) |
Make rs17204952(C;T) |
Make rs17204952(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 15 |
Position | 61188522 |
Gene | RORA |
is a | snp |
is | mentioned by |
dbSNP | rs17204952 |
dbSNP (classic) | rs17204952 |
ClinGen | rs17204952 |
ebi | rs17204952 |
HLI | rs17204952 |
Exac | rs17204952 |
Gnomad | rs17204952 |
Varsome | rs17204952 |
LitVar | rs17204952 |
Map | rs17204952 |
PheGenI | rs17204952 |
Biobank | rs17204952 |
1000 genomes | rs17204952 |
hgdp | rs17204952 |
ensembl | rs17204952 |
geneview | rs17204952 |
scholar | rs17204952 |
rs17204952 | |
pharmgkb | rs17204952 |
gwascentral | rs17204952 |
openSNP | rs17204952 |
23andMe | rs17204952 |
SNPshot | rs17204952 |
SNPdbe | rs17204952 |
MSV3d | rs17204952 |
GWAS Ctlg | rs17204952 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 29313974] Genetic variants in RORA and DNMT1 associated with cutaneous melanoma survival.