Variant #0001236344 (NC_000001.10:g.229693846A>C, NC_000001.10(NM_012089.2):c.517+37T>G (ABCB10))
Chromosome |
1 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.229693846A>C |
DB-ID |
- |
dbSNP ID |
rs4148757 |
gnomAD frequency |
1213/5776 |
gnomAD homozygote count |
142/1817 |
Average frequency (gnomAD v.2.1.1) |
0.21001 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
|
|