Variant #0001898469 (NC_000002.11:g.169828603A>G, NM_003742.2:c.1435-43delTinsC (ABCB11))
| Chromosome |
2 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.169828603A>G |
| DB-ID |
- |
| dbSNP ID |
rs112354931 |
| gnomAD frequency |
270/217352 |
| gnomAD homozygote count |
3/108409 |
| Average frequency (gnomAD v.2.1.1) |
0.00124 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
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