{{Rsnum
|rsid=1802959
|Chromosome=14
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SERPINA1
|position=94378628
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SERPINA1
}}{{omim
|id=107400
|rsnum=1802959
|variant=0029
}}

{{ClinVar
|rsid=1802959
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=94844965
|CHROM=14
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=SERPINA1:5265
|GENE_NAME=SERPINA1
|GENE_ID=5265
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.94844965C>T
|CLNORIGIN=0
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000019596.1
|CLNDBN=PI W(BETHESDA)
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=107400.0029
|Disease=PI W(BETHESDA)
}}

{{PMID|2185272|OA=1
}} Alpha 1-antitrypsin deficiency, emphysema, and liver disease. Genetic basis and strategies for therapy.

{{PMID|2240842}} Molecular analysis of the heterogeneity among the P-family of alpha-1-antitrypsin alleles.

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}