Variant #0011193564 (NC_000019.9:g.1881468G>C, NM_031213.3:c.98C>G (ABHD17A))
Chromosome |
19 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1881468G>C |
DB-ID |
- |
dbSNP ID |
rs530031473 |
gnomAD frequency |
7/232010 |
gnomAD homozygote count |
0/115998 |
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
|
|