Variant #0012964526 (NC_000023.10:g.74334640T>C, NM_004299.4:c.198A>G (ABCB7))
| Chromosome |
X |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.74334640T>C |
| DB-ID |
- |
| dbSNP ID |
rs774151733 |
| gnomAD frequency |
12/177912 |
| gnomAD homozygote count |
0/122317 |
| 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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