Gene: HBB ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11549407
rs11549407
HBB
A 0.700 CausalMutation CLINVAR

dbSNP: rs33915217
rs33915217
HBB
G 0.700 CausalMutation CLINVAR

dbSNP: rs33941377
rs33941377
HBB
T 0.700 CausalMutation CLINVAR

dbSNP: rs33944208
rs33944208
HBB
T 0.700 GeneticVariation CLINVAR

dbSNP: rs33945777
rs33945777
HBB
T 0.700 CausalMutation CLINVAR

dbSNP: rs33971440
rs33971440
HBB
T 0.700 CausalMutation CLINVAR

dbSNP: rs33986703
rs33986703
HBB
A 0.700 CausalMutation CLINVAR

dbSNP: rs34598529
rs34598529
HBB
C 0.700 CausalMutation CLINVAR

dbSNP: rs34690599
rs34690599
HBB
C 0.700 CausalMutation CLINVAR

dbSNP: rs35004220
rs35004220
HBB
T 0.700 CausalMutation CLINVAR

dbSNP: rs35724775
rs35724775
HBB
G 0.700 CausalMutation CLINVAR

dbSNP: rs33925391
rs33925391
HBB
0.010 GeneticVariation BEFREE Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia. 1463768

1992
dbSNP: rs35802118
rs35802118
HBB
0.010 GeneticVariation BEFREE Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia. 1463768

1992
dbSNP: rs63750022
rs63750022
HBB
0.010 GeneticVariation BEFREE Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia. 1463768

1992