Variant #0009611694 (NC_000016.9:g.2378444A>T, NC_000016.9(NM_001089.2):c.-27+10T>A (ABCA3))
| Chromosome |
16 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2378444A>T |
| DB-ID |
- |
| dbSNP ID |
rs28517480 |
| gnomAD frequency |
723/193230 |
| gnomAD homozygote count |
12/95903 |
| 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
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