Variant #0000061459 (NC_000002.11:g.233633460G>A, NM_002242.4:c.524C>T (KCNJ13))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.233633460G>A |
| DNA change (hg38) |
g.232768750G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
KCNJ13_000008 See all 2 reported entries |
| Variant remarks |
212/670 recessive retianl disease, 109/382 control chromosomes |
| Reference |
PubMed: Sergouniotis 2011 |
| ClinVar ID |
- |
| dbSNP ID |
rs1801251 |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
321/1052 chromosomes |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.34999 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2015-03-14 20:45:13 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
|