rs30168
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs30168(A;A) |
| Make rs30168(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 13718980 |
| Gene | DNAH5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs30168 |
| dbSNP (classic) | rs30168 |
| ClinGen | rs30168 |
| ebi | rs30168 |
| HLI | rs30168 |
| Exac | rs30168 |
| Gnomad | rs30168 |
| Varsome | rs30168 |
| LitVar | rs30168 |
| Map | rs30168 |
| PheGenI | rs30168 |
| Biobank | rs30168 |
| 1000 genomes | rs30168 |
| hgdp | rs30168 |
| ensembl | rs30168 |
| geneview | rs30168 |
| scholar | rs30168 |
| rs30168 | |
| pharmgkb | rs30168 |
| gwascentral | rs30168 |
| openSNP | rs30168 |
| 23andMe | rs30168 |
| SNPshot | rs30168 |
| SNPdbe | rs30168 |
| MSV3d | rs30168 |
| GWAS Ctlg | rs30168 |
| GMAF | 0.4421 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19197363
] A genome-wide investigation of SNPs and CNVs in schizophrenia.
| ClinVar | |
|---|---|
| Risk | rs30168(A;A) rs30168(C;C) rs30168(T;T) |
| Alt | rs30168(A;A) rs30168(C;C) rs30168(T;T) |
| Reference | Rs30168(G;G) |
| Significance | Non-pathogenic |
| Disease | not specified Primary ciliary dyskinesia |
| Variation | info |
| Gene | DNAH5 |
| CLNDBN | not specified Primary ciliary dyskinesia |
| Reversed | 0 |
| HGVS | NC_000005.9:g.13719089G>A |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000155503.2, RCV000265989.1, |
