Variant #0000603957 (NC_000011.9:g.?, HBB(NM_000518.4):c.?)
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.? |
DNA change (hg38) |
- |
Published as |
South East Asian (SEA) deletion (27 kb deletion) |
ISCN |
- |
DB-ID |
DRD4_000002 See all 167 reported entries |
Variant remarks |
β-thalassaemia, Haemolytic anaemia, Ineffective erythropoiesis |
Reference |
IthaNet-2126 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
Owner |
IthaNet - Petros Kountouris |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Variant on transcripts
|
|