{{Rsnum
|rsid=121907948
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SERPING1
|position=57614475
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SERPING1
}}{{omim
|id=606860
|rsnum=121907948
|variant=0003
}}{{ClinVar
|rsid=121907948
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=57381948
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=SERPING1:710
|GENE_NAME=SERPING1
|GENE_ID=710
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.57381948G>A; NC_000011.9:g.57381948G>T
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=606860.0003; VAR_007021
|CLNSIG=5
|CLNCUI=C1862892
|CLNDBN=Hereditary angioedema, type II; not provided
|Disease=Hereditary angioedema; not provided
|CLNACC=RCV000004152.1; RCV000059085.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1862892
}}{{PMID Auto
|PMID=22994404
|Title=Mutational spectrum and geno-phenotype correlation in Chinese families with hereditary angioedema.
}}