Variant #0000586389 (NC_000001.10:g.94476990C>T, NM_000350.2:c.5461-49delGinsA (ABCA4))
| Chromosome |
1 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94476990C>T |
| DB-ID |
- |
| dbSNP ID |
rs281865393 |
| gnomAD frequency |
7/235354 |
| gnomAD homozygote count |
0/117634 |
| Average frequency (gnomAD v.2.1.1) |
3.0E-5 View details |
| Database submission license |
No license selected |
| Created by |
LOVD |
| Date created |
2017-02-27 00:00:00 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
|
|