{{Rsnum
|rsid = 34131035
|Status = Merged
|Merged = 863931
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=1
|position=158642446
|Gene=SPTA1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SPTA1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 11.5 | 54.0 | 34.5
| HCB | 13.1 | 47.4 | 39.4
| JPT | 14.2 | 54.0 | 31.9
| YRI | 6.8 | 43.5 | 49.7
| ASW | 3.5 | 42.1 | 54.4
| CHB | 13.1 | 47.4 | 39.4
| CHD | 13.0 | 41.7 | 45.4
| GIH | 34.7 | 42.6 | 22.8
| LWK | 6.4 | 31.8 | 61.8
| MEX | 25.9 | 53.4 | 20.7
| MKK | 10.9 | 46.2 | 42.9
| TSI | 24.5 | 44.1 | 31.4
| HapMapRevision=28
}}{{Venter SNP
|rsid=34131035
|allele=G
|frequency=
|uid=1103675236084
|type=heterozygous_SNP
|hugo=SPTA1
|ensembl gene=ENSG00000163554
|ensembl transcript=ENST00000368148
|sift=TOLERATED
|disease=Defects in SPTA1 are the cause of spherocytosis type III (SPH3) (MIM:270970). SPH3 is a disorder characterized by severe hemolytic anemia. Inheritance is autosomal recessive.
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | Affy500k}}