Variant #0012461608 (NC_000021.8:g.43693579C>T, NM_207628.1:c.471+34delCinsT (ABCG1))
Chromosome |
21 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.43693579C>T |
DB-ID |
- |
dbSNP ID |
rs752770699 |
gnomAD frequency |
4/226130 |
gnomAD homozygote count |
0/113060 |
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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