Variant #0000588889 (NC_000001.10:g.94586598C>G, NM_000350.2:c.4G>C (ABCA4))
Chromosome |
1 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94586598C>G |
DB-ID |
- |
dbSNP ID |
rs751669641 |
gnomAD frequency |
1/246254 |
gnomAD homozygote count |
0/123126 |
Average frequency (gnomAD v.2.1.1) |
0 View details |
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
|
|