Variant #0007859636 (NC_000012.11:g.22089465A>G, NC_000012.11(NM_005691.2):c.142+2T>C (ABCC9))
Chromosome |
12 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.22089465A>G |
DB-ID |
- |
dbSNP ID |
rs373876069 |
gnomAD frequency |
1/244758 |
gnomAD homozygote count |
0/122378 |
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
|
|