Variant #0000000206 (NC_000002.11:g.60719970C>A, BCL11A(NM_022893.3):c.386-24002G>T)
| Chromosome |
2 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
Substitution |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.60719970C>A |
| Reference |
dbSNP |
| DB-ID |
BCL11A_000013 See all 2 reported entries |
| Frequency |
35/60 |
| Variant remarks |
Correlation Between Fetal Hemoglobin and Single Nucleotide Polymorphism at BCL11A Gene in major beta-thalassemia Patients in Guangxi province. |
| ClassClinical |
Likely benign |
| 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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