Variant #0000588621 (NC_000001.10:g.94564552A>C, NM_000350.2:c.571-5delTinsG (ABCA4))
Chromosome |
1 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94564552A>C |
DB-ID |
- |
dbSNP ID |
rs200013776 |
gnomAD frequency |
21/230548 |
gnomAD homozygote count |
0/115252 |
Average frequency (gnomAD v.2.1.1) |
9.0E-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
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