Variant #0006099962 (NC_000009.11:g.99417331C>T, NC_000009.11(NM_153698.1):c.192+41G>A (AAED1))
Chromosome |
9 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.99417331C>T |
DB-ID |
- |
dbSNP ID |
rs57656890 |
gnomAD frequency |
519/68448 |
gnomAD homozygote count |
41/33746 |
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
|
|