Variant #0000590196 (NC_000001.10:g.94884000_94884001insCGT, NM_002858.3:c.-35_-34insCGT (ABCD3))
Chromosome |
1 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94884000_94884001insCGT |
DB-ID |
- |
dbSNP ID |
rs753091516 |
gnomAD frequency |
1/180448 |
gnomAD homozygote count |
0/90217 |
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
|
|