Variant #0005046548 (NC_000007.13:g.87104716T>C, NM_018849.2:c.66A>G (ABCB4))
Chromosome |
7 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.87104716T>C |
DB-ID |
- |
dbSNP ID |
rs759437240 |
gnomAD frequency |
10/246228 |
gnomAD homozygote count |
0/123104 |
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
|
|