Variant #0001499193 (NC_000002.11:g.44065849T>C, NM_022437.2:c.-344T>C (ABCG8))
Chromosome |
2 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.44065849T>C |
DB-ID |
- |
dbSNP ID |
rs56289199 |
gnomAD frequency |
28/238954 |
gnomAD homozygote count |
0/119449 |
Average frequency (gnomAD v.2.1.1) |
0.00012 View details |
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
|
|