{{Rsnum
|rsid=28358582
|Gene=ANKRD20A19P
|Chromosome=MT
|position=3308
|Orientation=plus
|GMAF=0.02713
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MT-ND1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 17.5 | 0.0 | 82.5
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{ClinVar
|ALT=C,G
|CAF=0.9729; 0.02713; .
|CHROM=MT
|CLNACC=RCV000010379.1; RCV000010380.3; RCV000010381.1
|CLNALLE=1; 2
|CLNDBN=Carcinoma of colon; Sudden infant death syndrome
|CLNDSDB=MedGen:SNOMED_CT; MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0699790:269533000; C0038644:272120:51178009
|CLNHGVS=NC_012920.1:m.3308T>C; NC_012920.1:m.3308T>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=516000.0007; 516000.0008
|COMMON=1
|Disease=Carcinoma of colon; Sudden infant death syndrome
|FwdALT=C,G
|FwdREF=T
|REF=T
|RSPOS=3308
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;VLD;G5;HD;GNO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000150502110100
|WGT=0
|dbSNPBuildID=125
|rsid=28358582
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}