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
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