Variant #0000586389 (NC_000001.10:g.94476990C>T, NM_000350.2:c.5461-49delGinsA (ABCA4))
Chromosome |
1 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94476990C>T |
DB-ID |
- |
dbSNP ID |
rs281865393 |
gnomAD frequency |
7/235354 |
gnomAD homozygote count |
0/117634 |
Average frequency (gnomAD v.2.1.1) |
3.0E-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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