Variant #0007804193 (NC_000012.11:g.9221429G>C, NM_000014.4:c.4273C>G (A2M))
| Chromosome |
12 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.9221429G>C |
| DB-ID |
- |
| dbSNP ID |
rs766672959 |
| gnomAD frequency |
3/220452 |
| gnomAD homozygote count |
0/110223 |
| 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
|
|