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: rs281860601
rs281860601
HBG1
A 0.700 CausalMutation CLINVAR

dbSNP: rs334
rs334
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: rs34809449
rs34809449
HBG2
T 0.700 CausalMutation CLINVAR

dbSNP: rs34809449
rs34809449
HBG2
A 0.700 CausalMutation CLINVAR

dbSNP: rs35004220
rs35004220
HBB
T 0.700 CausalMutation CLINVAR

dbSNP: rs35321913
rs35321913
HBG1
C 0.700 CausalMutation CLINVAR

dbSNP: rs35378915
rs35378915
HBG1
T 0.700 CausalMutation CLINVAR

dbSNP: rs35617911
rs35617911
HBG2
C 0.700 CausalMutation CLINVAR

dbSNP: rs35710727
rs35710727
HBG1
G 0.700 CausalMutation CLINVAR

dbSNP: rs35724775
rs35724775
HBB
G 0.700 CausalMutation CLINVAR

dbSNP: rs35983258
rs35983258
HBG1
A 0.700 CausalMutation CLINVAR

dbSNP: rs63750654
rs63750654
HBG2
G 0.700 CausalMutation CLINVAR