rs45430
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs45430(A;A) |
Make rs45430(A;G) |
Make rs45430(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 41374154 |
Gene | MX2 |
is a | snp |
is | mentioned by |
dbSNP | rs45430 |
dbSNP (classic) | rs45430 |
ClinGen | rs45430 |
ebi | rs45430 |
HLI | rs45430 |
Exac | rs45430 |
Gnomad | rs45430 |
Varsome | rs45430 |
LitVar | rs45430 |
Map | rs45430 |
PheGenI | rs45430 |
Biobank | rs45430 |
1000 genomes | rs45430 |
hgdp | rs45430 |
ensembl | rs45430 |
geneview | rs45430 |
scholar | rs45430 |
rs45430 | |
pharmgkb | rs45430 |
gwascentral | rs45430 |
openSNP | rs45430 |
23andMe | rs45430 |
SNPshot | rs45430 |
SNPdbe | rs45430 |
MSV3d | rs45430 |
GWAS Ctlg | rs45430 |
GMAF | 0.4417 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21983787] |
Trait | |
Title | Genome-wide association study identifies three new melanoma susceptibility loci. |
Risk Allele | |
P-val | 3E-9 |
Odds Ratio | 1.1400 None |
[PMID 25837821] Inherited genetic variants associated with occurrence of multiple primary melanoma