Variant #0007642346 (NC_000011.9:g.119020630T>C, NC_000011.9(NM_001142505.1):c.-12-34T>C (ABCG4))
Chromosome |
11 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.119020630T>C |
DB-ID |
- |
dbSNP ID |
rs767408403 |
gnomAD frequency |
2/216942 |
gnomAD homozygote count |
0/108469 |
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
|
|