Variant #0001899020 (NC_000002.11:g.169873326del, NC_000002.11(NM_003742.2):c.77-17delA (ABCB11))
| Chromosome |
2 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.169873326del |
| DB-ID |
- |
| dbSNP ID |
rs11568375 |
| gnomAD frequency |
913/210198 |
| gnomAD homozygote count |
10/104196 |
| Average frequency (gnomAD v.2.1.1) |
0.00434 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
|
|