Variant #0000588861 (NC_000001.10:g.94586506C>T, NC_000001.10(NM_000350.2):c.66+30G>A (ABCA4))
Chromosome |
1 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94586506C>T |
DB-ID |
- |
dbSNP ID |
rs756060783 |
gnomAD frequency |
2/244848 |
gnomAD homozygote count |
0/122421 |
Average frequency (gnomAD v.2.1.1) |
1.0E-5 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
|
|