rs3750344
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs3750344(A;G) |
| Make rs3750344(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 98578034 |
| Gene | GABBR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3750344 |
| dbSNP (classic) | rs3750344 |
| ClinGen | rs3750344 |
| ebi | rs3750344 |
| HLI | rs3750344 |
| Exac | rs3750344 |
| Gnomad | rs3750344 |
| Varsome | rs3750344 |
| LitVar | rs3750344 |
| Map | rs3750344 |
| PheGenI | rs3750344 |
| Biobank | rs3750344 |
| 1000 genomes | rs3750344 |
| hgdp | rs3750344 |
| ensembl | rs3750344 |
| geneview | rs3750344 |
| scholar | rs3750344 |
| rs3750344 | |
| pharmgkb | rs3750344 |
| gwascentral | rs3750344 |
| openSNP | rs3750344 |
| 23andMe | rs3750344 |
| SNPshot | rs3750344 |
| SNPdbe | rs3750344 |
| MSV3d | rs3750344 |
| GWAS Ctlg | rs3750344 |
| GMAF | 0.1795 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 15759211
] Associated with Nicotine Dependence as part of several haplotypes, based on a study of 1,000+ subjects including both African-Americans and European-Americans.
Interestingly, the risk allele varies between populations. Among African-Americans, the haplotype C-C-G of rs2491397-rs2184026-rs3750344 had a significant positive association with nicotine dependence. Among European-Americans, for rs1435252-rs3780422-rs2779562-rs3750344, the C-A-C-A haplotype was positively associated with nicotine dependence while the T-A-T-A haplotype was negatively associated.[PMID 15759211
]
[PMID 19763258
] Association and interaction analyses of GABBR1 and GABBR2 with nicotine dependence in European- and African-American populations.
| ClinVar | |
|---|---|
| Risk | rs3750344(G;G) |
| Alt | rs3750344(G;G) |
| Reference | Rs3750344(A;A) |
| Significance | Other |
| Disease | Tobacco addiction |
| Variation | info |
| Gene | GABBR2 |
| CLNDBN | Tobacco addiction, susceptibility to |
| Reversed | 1 |
| HGVS | NC_000009.11:g.101340316T>C |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000003495.1, |
