Variant #0000590192 (NC_000001.10:g.94883997C>T, NM_002858.3:c.-38C>T (ABCD3))
Chromosome |
1 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94883997C>T |
DB-ID |
- |
dbSNP ID |
rs760091843 |
gnomAD frequency |
5/176038 |
gnomAD homozygote count |
0/88014 |
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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