Variant #0000000238 (NC_000011.9:g.5193974_5273251del, HBG1(NM_000559.2):c.-2217_*75615del)
Chromosome |
11 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Deletion |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5193974_5273251del |
Reference |
Kosteas et al |
DB-ID |
HBD_000022 See all 3 reported entries |
Frequency |
- |
Variant remarks |
HPFH-6 |
ClassClinical |
Pathogenic |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
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