Variant #0000000120 (NC_000011.9:g.5277291C>T, HBG2(NM_000184.2):c.-1333G>A)
| Individual ID |
00000017, 00000049, 00000104, 00000155, 00000362, 00000390, 00000568, 00000636, 00000638, 00000738, 00000805, 00001086, 00001138, 00001292, 00001564, 00001686, 00001749, 00001755, 00002003, 00002050 |
| Chromosome |
11 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Type |
Substitution |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5277291C>T |
| Reference |
GenBank;dbSNP |
| DB-ID |
HBG2_000011 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
|
|