{{Rsnum
|rsid=121918647
|Chromosome=14
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SPTB
|position=64767829
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SPTB
}}{{omim
|id=182870
|rsnum=121918647
|variant=0008
}}{{ClinVar
|rsid=121918647
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=65234547
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SPTB:6710
|GENE_NAME=SPTB
|GENE_ID=6710
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.65234547G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=182870.0008
|CLNSIG=5
|CLNCUI=C0520739
|CLNDBN=Hereditary pyropoikilocytosis; Elliptocytosis 3
|Disease=Hereditary pyropoikilocytosis; Elliptocytosis 3
|CLNACC=RCV000013686.16; RCV000013687.22
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:SNOMED_CT; MedGen
|CLNDSDBID=C0520739:266140:9434008; C1866810
}}