Variant #0000000101 (NC_000011.9:g.5270002G>A, HBG1(NM_000559.2):c.316-285C>T)
Individual ID |
00000460, 00000913, 00001780, 00001965, 00001997 |
Chromosome |
11 |
Allele |
Both (homozygous) |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Type |
Deletion |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5270002G>A |
Reference |
GenBank;dbSNP |
DB-ID |
HBG1_000003 See all 2 reported entries |
Frequency |
- |
Variant remarks |
- |
ClassClinical |
uncertain significance |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
Screenings
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