rs35908728
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | |
| (G;G) | 0 | common in complete genomics |
| Make rs35908728(A;A) |
| Make rs35908728(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 20 |
| Position | 62819953 |
| Gene | COL9A3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35908728 |
| dbSNP (classic) | rs35908728 |
| ClinGen | rs35908728 |
| ebi | rs35908728 |
| HLI | rs35908728 |
| Exac | rs35908728 |
| Gnomad | rs35908728 |
| Varsome | rs35908728 |
| LitVar | rs35908728 |
| Map | rs35908728 |
| PheGenI | rs35908728 |
| Biobank | rs35908728 |
| 1000 genomes | rs35908728 |
| hgdp | rs35908728 |
| ensembl | rs35908728 |
| geneview | rs35908728 |
| scholar | rs35908728 |
| rs35908728 | |
| pharmgkb | rs35908728 |
| gwascentral | rs35908728 |
| openSNP | rs35908728 |
| 23andMe | rs35908728 |
| SNPshot | rs35908728 |
| SNPdbe | rs35908728 |
| MSV3d | rs35908728 |
| GWAS Ctlg | rs35908728 |
| GMAF | 0.03444 |
| Max Magnitude | 0 |
This SNP currently serves only as a marker for a SNP known as Arg103Trp that lacks an rs# in dbSNP, but is 27 nucleotides away from rs35908728 in the COL9A3 gene.
For details, see the entry for lumbar disc disease.
| ClinVar | |
|---|---|
| Risk | rs35908728(A;A) |
| Alt | rs35908728(A;A) |
| Reference | Rs35908728(G;G) |
| Significance | Probable-non-pathogenic |
| Disease | not specified Multiple Epiphyseal Dysplasia |
| Variation | info |
| Gene | COL9A3 |
| CLNDBN | not specified Multiple Epiphyseal Dysplasia, Dominant |
| Reversed | 1 |
| HGVS | NC_000020.10:g.61451305C>T |
| CLNSRC | |
| CLNACC | RCV000249161.1, RCV000356406.1, |
