Variant #0001898997 (NC_000002.11:g.169870855A>G, NM_003742.2:c.108T>C (ABCB11))
Chromosome |
2 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.169870855A>G |
DB-ID |
- |
dbSNP ID |
rs3815675 |
gnomAD frequency |
7756/245806 |
gnomAD homozygote count |
821/115968 |
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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