Variant #0012146216 (NC_000020.10:g.25371135_25371142del, NC_000020.10(NM_015600.4):c.191+7_191+14del (ABHD12))
Chromosome |
20 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.25371135_25371142del |
DB-ID |
- |
dbSNP ID |
rs369626505 |
gnomAD frequency |
163/60010 |
gnomAD homozygote count |
0/29790 |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
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
|
|