Variant #0012964548 (NC_000023.10:g.74375987A>G, NM_004299.4:c.121T>C (ABCB7))
Chromosome |
X |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.74375987A>G |
DB-ID |
- |
dbSNP ID |
rs143380072 |
gnomAD frequency |
77/169042 |
gnomAD homozygote count |
1/113803 |
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
|
|