Variant #0007859626 (NC_000012.11:g.22089425A>G, NC_000012.11(NM_005691.2):c.142+42T>C (ABCC9))
Chromosome |
12 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.22089425A>G |
DB-ID |
- |
dbSNP ID |
rs182534835 |
gnomAD frequency |
1341/231320 |
gnomAD homozygote count |
7/114326 |
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
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