{{Rsnum
|rsid=28357970
|Gene=MT-ND1
|Chromosome=MT
|position=3796
|Orientation=plus
|GMAF=0.006548
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| 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
}}[[haplogroups]]

{{hgsnp
|alternate_names=A3796G
|sources={{PMID|17099056}}
|tree=PhyloTree
|tree_build=7
|ancestral_haplogroup=H1a
|derived_haplogroup=H1b
|ancestral_allele=A
|derived_allele=G
}}

{{ClinVar
|ALT=G,T
|CAF=0.9906; 0.006548; 0.002806
|CHROM=MT
|CLNACC=RCV000010382.3
|CLNALLE=1
|CLNDBN=Dystonia, adult-onset
|CLNDSDB=MedGen
|CLNDSDBID=C0752197
|CLNHGVS=NC_012920.1:m.3796A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=516000.0011
|COMMON=1
|Disease=Dystonia
|FwdALT=G,T
|FwdREF=A
|REF=A
|RSPOS=3796
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;HD;GNO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000502110100
|WGT=0
|dbSNPBuildID=125
|rsid=28357970
}}

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