{{Rsnum
|rsid = 34727075
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Gene = ANK1
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=8
|position=41692865
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ANK1
}}{{Venter SNP
|rsid=34727075
|allele=A
|frequency=
|uid=1103652304976
|type=heterozygous_SNP
|hugo=ANK1
|ensembl gene=ENSG00000029534
|ensembl transcript=ENST00000347528
|sift=TOLERATED
|disease=Defects in ANK1 are a cause of hereditary spherocytosis (HS) (MIM:182900). Inheritance can be autosomal dominant or recessive.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}