Variant #0000590226 (NC_000001.10:g.94884095C>T, NM_002858.3:c.61C>T (ABCD3))
Chromosome |
1 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94884095C>T |
DB-ID |
- |
dbSNP ID |
rs550594664 |
gnomAD frequency |
87/230676 |
gnomAD homozygote count |
0/115251 |
Average frequency (gnomAD v.2.1.1) |
0.00038 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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