Variant #0012461366 (NC_000021.8:g.43639408C>T, NC_000021.8(NM_207628.1):c.-24-6373C>T (ABCG1))
| Chromosome |
21 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.43639408C>T |
| DB-ID |
- |
| dbSNP ID |
rs377272380 |
| gnomAD frequency |
12/222262 |
| gnomAD homozygote count |
0/111118 |
| 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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