rs1981997
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1981997(A;A) |
| Make rs1981997(A;G) |
| Make rs1981997(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 45979401 |
| Gene | MAPT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1981997 |
| dbSNP (classic) | rs1981997 |
| ClinGen | rs1981997 |
| ebi | rs1981997 |
| HLI | rs1981997 |
| Exac | rs1981997 |
| Gnomad | rs1981997 |
| Varsome | rs1981997 |
| LitVar | rs1981997 |
| Map | rs1981997 |
| PheGenI | rs1981997 |
| Biobank | rs1981997 |
| 1000 genomes | rs1981997 |
| hgdp | rs1981997 |
| ensembl | rs1981997 |
| geneview | rs1981997 |
| scholar | rs1981997 |
| rs1981997 | |
| pharmgkb | rs1981997 |
| gwascentral | rs1981997 |
| openSNP | rs1981997 |
| 23andMe | rs1981997 |
| SNPshot | rs1981997 |
| SNPdbe | rs1981997 |
| MSV3d | rs1981997 |
| GWAS Ctlg | rs1981997 |
| GMAF | 0.1171 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23583980 ]
|
| Trait | Interstitial lung disease |
| Title | Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. |
| Risk Allele | G |
| P-val | 9E-14 |
| Odds Ratio | 1.41 [1.28-1.56] |
[PMID 18985386] Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
[PMID 20070850] Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
