Variant #0009456171 (NC_000015.9:g.89694936A>C, NM_007011.7:c.223A>C (ABHD2))
Chromosome |
15 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.89694936A>C |
DB-ID |
- |
dbSNP ID |
rs770265352 |
gnomAD frequency |
1/245832 |
gnomAD homozygote count |
0/122914 |
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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