rs1048101
| Orientation | minus |
| Stabilized | minus |
| Make rs1048101(C;C) |
| Make rs1048101(C;T) |
| Make rs1048101(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 26770511 |
| Gene | ADRA1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1048101 |
| dbSNP (classic) | rs1048101 |
| ClinGen | rs1048101 |
| ebi | rs1048101 |
| HLI | rs1048101 |
| Exac | rs1048101 |
| Gnomad | rs1048101 |
| Varsome | rs1048101 |
| LitVar | rs1048101 |
| Map | rs1048101 |
| PheGenI | rs1048101 |
| Biobank | rs1048101 |
| 1000 genomes | rs1048101 |
| hgdp | rs1048101 |
| ensembl | rs1048101 |
| geneview | rs1048101 |
| scholar | rs1048101 |
| rs1048101 | |
| pharmgkb | rs1048101 |
| gwascentral | rs1048101 |
| openSNP | rs1048101 |
| 23andMe | rs1048101 |
| SNPshot | rs1048101 |
| SNPdbe | rs1048101 |
| MSV3d | rs1048101 |
| GWAS Ctlg | rs1048101 |
| GMAF | 0.3604 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19565482] Association of adrenergic receptor gene polymorphisms with different fibromyalgia syndrome domains
[PMID 15900517
] Novel human alpha1a-adrenoceptor single nucleotide polymorphisms alter receptor pharmacology and biological function.
[PMID 16642433] Polymorphism in maternal LRP8 gene is associated with fetal growth.
[PMID 18444252] Neurotransmission and bipolar disorder: a systematic family-based association study.
[PMID 19102884] [Association between ADRA1A gene polymorphism and autoantibodies against the alpha1-adrenergic receptor in hypertensive patients.].
[PMID 19730237] Personalized medicine: genetic variation and loss of physiologic complexity are associated with mortality in 644 trauma patients.
[PMID 20173430] Frequencies of polymorphisms in cytokines, neurotransmitters and adrenergic receptors in patients with complex regional pain syndrome type I after distal radial fracture.
[PMID 29197114] The correlation between SNPs within the gene of adrenergic receptor and neuropeptide Y and risk of cervical vertigo.
