Variant #0004850767 (NC_000007.13:g.20662961G>C, NM_001163941.1:c.53G>C (ABCB5))
| Chromosome |
7 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.20662961G>C |
| DB-ID |
- |
| dbSNP ID |
rs185876249 |
| gnomAD frequency |
18/153966 |
| gnomAD homozygote count |
0/76965 |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| 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
|
|