rs1422795
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1422795(A;A) |
| Make rs1422795(A;G) |
| Make rs1422795(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 157509356 |
| Gene | ADAM19 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1422795 |
| dbSNP (classic) | rs1422795 |
| ClinGen | rs1422795 |
| ebi | rs1422795 |
| HLI | rs1422795 |
| Exac | rs1422795 |
| Gnomad | rs1422795 |
| Varsome | rs1422795 |
| LitVar | rs1422795 |
| Map | rs1422795 |
| PheGenI | rs1422795 |
| Biobank | rs1422795 |
| 1000 genomes | rs1422795 |
| hgdp | rs1422795 |
| ensembl | rs1422795 |
| geneview | rs1422795 |
| scholar | rs1422795 |
| rs1422795 | |
| pharmgkb | rs1422795 |
| gwascentral | rs1422795 |
| openSNP | rs1422795 |
| 23andMe | rs1422795 |
| SNPshot | rs1422795 |
| SNPdbe | rs1422795 |
| MSV3d | rs1422795 |
| GWAS Ctlg | rs1422795 |
| GMAF | 0.3783 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19319892
] A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees.
[PMID 20010835
] Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.
[PMID 21304900
] Individual and cumulative effects of GWAS susceptibility loci in lung cancer: associations after sub-phenotyping for COPD.
[PMID 24951661
] ADAM19 and HTR4 Variants and Pulmonary Function: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 5
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- 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 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
