{{Rsnum
|rsid=857721
|Gene=SPTA1
|Chromosome=1
|position=158642758
|Orientation=plus
|GMAF=0.2686
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=SPTA1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 8.8 | 46.0 | 45.1
| HCB | 13.1 | 50.4 | 36.5
| JPT | 13.3 | 47.8 | 38.9
| YRI | 1.4 | 8.2 | 90.5
| ASW | 0.0 | 22.8 | 77.2
| CHB | 13.1 | 50.4 | 36.5
| CHD | 23.6 | 52.8 | 23.6
| GIH | 7.9 | 23.8 | 68.3
| LWK | 1.8 | 20.2 | 78.0
| MEX | 6.9 | 37.9 | 55.2
| MKK | 3.2 | 27.7 | 69.0
| TSI | 2.0 | 45.5 | 52.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19862010
|Trait=Other erythrocyte phenotypes
|Title=Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
|RiskAllele=A
|Pval=1E-10
|OR=0
|ORtxt=[0.001-0.002] g/dl decrease
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs857721
|overall_frequency_n=30
|overall_frequency_d=128
|overall_frequency=0.234375
|n_genomes=21
|n_genomes_annotated=0
|n_haplomes=25
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}