Variant #0001236338 (NC_000001.10:g.229685207T>C, NC_000001.10(NM_012089.2):c.518-26A>G (ABCB10))
Chromosome |
1 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.229685207T>C |
DB-ID |
- |
dbSNP ID |
rs750190303 |
gnomAD frequency |
7/216952 |
gnomAD homozygote count |
0/108469 |
Average frequency (gnomAD v.2.1.1) |
3.0E-5 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
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