Variant #0006378468 (NC_000009.11:g.139926492C>A, NM_001606.4:c.-3900G>T (ABCA2))
Chromosome |
9 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.139926492C>A |
DB-ID |
- |
dbSNP ID |
rs771419766 |
gnomAD frequency |
2/245108 |
gnomAD homozygote count |
0/122552 |
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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