rs1990595
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1990595(A;A) |
| Make rs1990595(A;C) |
| Make rs1990595(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 81106042 |
| Gene | LOC101928462, TSHR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1990595 |
| dbSNP (classic) | rs1990595 |
| ClinGen | rs1990595 |
| ebi | rs1990595 |
| HLI | rs1990595 |
| Exac | rs1990595 |
| Gnomad | rs1990595 |
| Varsome | rs1990595 |
| LitVar | rs1990595 |
| Map | rs1990595 |
| PheGenI | rs1990595 |
| Biobank | rs1990595 |
| 1000 genomes | rs1990595 |
| hgdp | rs1990595 |
| ensembl | rs1990595 |
| geneview | rs1990595 |
| scholar | rs1990595 |
| rs1990595 | |
| pharmgkb | rs1990595 |
| gwascentral | rs1990595 |
| openSNP | rs1990595 |
| 23andMe | rs1990595 |
| SNPshot | rs1990595 |
| SNPdbe | rs1990595 |
| MSV3d | rs1990595 |
| GWAS Ctlg | rs1990595 |
| GMAF | 0.4229 |
| Max Magnitude | 0 |
[PMID 22673349] Association between thyroid stimulating hormone receptor gene intron polymorphisms and autoimmune thyroid disease in a Chinese Han population
