Variant #0007804162 (NC_000012.11:g.9220729G>A, NC_000012.11(NM_000014.4):c.4408+50C>T (A2M))
Chromosome |
12 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.9220729G>A |
DB-ID |
- |
dbSNP ID |
rs7955940 |
gnomAD frequency |
76663/233950 |
gnomAD homozygote count |
14016/54328 |
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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