{{Rsnum
|rsid=121918644
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SPTA1
|position=158685229
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SPTA1
}}{{omim
|id=182860
|rsnum=121918644
|variant=0017
}}{{ClinVar
|rsid=121918644
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=158685229
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=SPTA1:6708
|GENE_NAME=SPTA1
|GENE_ID=6708
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.158685229T>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_003126.2:c.143A>G; 182860.0017
|CLNSIG=5
|CLNCUI=C0520739
|CLNDBN=Hereditary pyropoikilocytosis
|Disease=Hereditary pyropoikilocytosis
|CLNACC=RCV000013716.23
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0520739:266140:9434008
}}