Variant #0011167896 (NC_000019.9:g.1036631T>C, NM_019112.3:c.-3702T>C (ABCA7))
| Chromosome |
19 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1036631T>C |
| DB-ID |
- |
| dbSNP ID |
rs11672916 |
| gnomAD frequency |
37250/238674 |
| gnomAD homozygote count |
3302/85389 |
| 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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