rs1990932
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1990932(A;A) |
| Make rs1990932(A;G) |
| Make rs1990932(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 45937042 |
| Gene | NOVA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1990932 |
| dbSNP (classic) | rs1990932 |
| ClinGen | rs1990932 |
| ebi | rs1990932 |
| HLI | rs1990932 |
| Exac | rs1990932 |
| Gnomad | rs1990932 |
| Varsome | rs1990932 |
| LitVar | rs1990932 |
| Map | rs1990932 |
| PheGenI | rs1990932 |
| Biobank | rs1990932 |
| 1000 genomes | rs1990932 |
| hgdp | rs1990932 |
| ensembl | rs1990932 |
| geneview | rs1990932 |
| scholar | rs1990932 |
| rs1990932 | |
| pharmgkb | rs1990932 |
| gwascentral | rs1990932 |
| openSNP | rs1990932 |
| 23andMe | rs1990932 |
| SNPshot | rs1990932 |
| SNPdbe | rs1990932 |
| MSV3d | rs1990932 |
| GWAS Ctlg | rs1990932 |
| GMAF | 0.4366 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20133464] Identification of a Second Kindred with Familial Hypocalciuric Hypercalcemia Type 3 (FHH3) Narrows Localization to a <3.5 Megabase Pair Region on Chromosome 19q13.3
