Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28929474
rs28929474
T 0.710 CausalMutation CLINVAR DNA restriction fragments associated with alpha 1-antitrypsin indicate a single origin for deficiency allele PI Z. 2989709

1985

dbSNP: rs17580
rs17580
A 0.710 CausalMutation CLINVAR

dbSNP: rs55819880
rs55819880
A 0.700 CausalMutation CLINVAR PI*S(iiyama), a deficiency gene of alpha 1-antitrypsin: evidence for the occurrence in western Japan. 8358043

1993

dbSNP: rs11558261
rs11558261
T 0.700 CausalMutation CLINVAR Molecular characterisation of two alpha-1-antitrypsin deficiency variants: proteinase inhibitor (Pi) Null(Newport) (Gly115----Ser) and (Pi) Z Wrexham (Ser-19----Leu). 2227940

1990

dbSNP: rs28931568
rs28931568
T 0.700 CausalMutation CLINVAR Molecular basis of alpha 1-antitrypsin deficiency and emphysema associated with the alpha 1-antitrypsin Mmineral springs allele. 1967187

1990

dbSNP: rs28931572
rs28931572
T 0.700 CausalMutation CLINVAR A null deficiency allele of alpha 1-antitrypsin, QOludwigshafen, with altered tertiary structure. 2254451

1990

dbSNP: rs121912714
rs121912714
A 0.700 CausalMutation CLINVAR The deficient alpha-I-antitrypsin phenotype PI P is associated with an A-to-T transversion in exon III of the gene. 2787118

1989

dbSNP: rs28931570
rs28931570
A 0.700 CausalMutation CLINVAR Molecular characterisation of three alpha-1-antitrypsin deficiency variants: proteinase inhibitor (Pi) nullcardiff (Asp256----Val); PiMmalton (Phe51----deletion) and PiI (Arg39----Cys). 2606478

1989

dbSNP: rs775982338
rs775982338
G 0.700 CausalMutation CLINVAR In-frame single codon deletion in the Mmalton deficiency allele of alpha 1-antitrypsin. 2786335

1989

dbSNP: rs28931569
rs28931569
G 0.700 CausalMutation CLINVAR "Characterization of the gene and protein of the alpha 1-antitrypsin ""deficiency"" allele Mprocida." 3262617

1988

dbSNP: rs121912713
rs121912713
C 0.700 CausalMutation CLINVAR

dbSNP: rs1457464431
rs1457464431
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555367891
rs1555367891
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555367892
rs1555367892
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555367896
rs1555367896
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555369172
rs1555369172
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555369299
rs1555369299
A 0.700 CausalMutation CLINVAR

dbSNP: rs199422209
rs199422209
A 0.700 CausalMutation CLINVAR

dbSNP: rs199422211
rs199422211
A 0.700 CausalMutation CLINVAR

dbSNP: rs267606950
rs267606950
C 0.700 CausalMutation CLINVAR

dbSNP: rs28931569
rs28931569
G 0.700 GeneticVariation CLINVAR

dbSNP: rs751235320
rs751235320
A 0.700 CausalMutation CLINVAR

dbSNP: rs756773408
rs756773408
A 0.700 GeneticVariation CLINVAR

dbSNP: rs764325655
rs764325655
C 0.700 CausalMutation CLINVAR