Variant #0012202884 (NC_000020.10:g.34827799C>T, NM_001271874.1:c.9C>T (AAR2))
Chromosome |
20 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.34827799C>T |
DB-ID |
- |
dbSNP ID |
rs768243727 |
gnomAD frequency |
4/233434 |
gnomAD homozygote count |
0/116713 |
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
|
|