rs6478241
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6478241(A;A) |
| Make rs6478241(A;G) |
| Make rs6478241(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 116490350 |
| Gene | ASTN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6478241 |
| dbSNP (classic) | rs6478241 |
| ClinGen | rs6478241 |
| ebi | rs6478241 |
| HLI | rs6478241 |
| Exac | rs6478241 |
| Gnomad | rs6478241 |
| Varsome | rs6478241 |
| LitVar | rs6478241 |
| Map | rs6478241 |
| PheGenI | rs6478241 |
| Biobank | rs6478241 |
| 1000 genomes | rs6478241 |
| hgdp | rs6478241 |
| ensembl | rs6478241 |
| geneview | rs6478241 |
| scholar | rs6478241 |
| rs6478241 | |
| pharmgkb | rs6478241 |
| gwascentral | rs6478241 |
| openSNP | rs6478241 |
| 23andMe | rs6478241 |
| SNPshot | rs6478241 |
| SNPdbe | rs6478241 |
| MSV3d | rs6478241 |
| GWAS Ctlg | rs6478241 |
| GMAF | 0.4522 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22683712 |
| Trait | |
| Title | Genome-wide association analysis identifies susceptibility loci for migraine without aura. |
| Risk Allele | A |
| P-val | 4E-8 |
| Odds Ratio | 1.1600 None |
| GWAS snp | |
|---|---|
| PMID | [PMID 23793025 |
| Trait | Migraine - clinic-based |
| Title | Genome-wide meta-analysis identifies new susceptibility loci for migraine. |
| Risk Allele | A |
| P-val | 1E-9 |
| Odds Ratio | 1.16 [1.11-1.22] |
[PMID 24674449
] A replication study of GWAS findings in migraine identifies association in a Swedish case-control sample
[PMID 25179292] Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies
[PMID 30256423] Using a Genetic Risk Score Approach to Predict Headache Response to Triptans in Migraine Without Aura.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 9
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip 23andMe v5
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2c
- On chip Ancestry v2d
