{{Rsnum
|rsid=28357980
|Gene=MT-ND2
|Chromosome=MT
|position=4917
|Orientation=plus
|GMAF=0.03461
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MT-CO1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 89.1 | 1.6 | 9.4
| 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
}}Also known as mitochondrial SNP 4917G.

[http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0002091 PLoS] This SNP predicts the presence of [[age related macular degeneration]] (odds ratio = 2.16, CI: 1.20-3.91, p = 0.01).

[http://www.thinkgene.com/cells-power-plant-genes-raise-vision-disorder-risk/ ThinkGene] coverage

{{ClinVar
|ALT=G
|CAF=0.9654; 0.03461
|CHROM=MT
|CLNACC=RCV000010364.1
|CLNALLE=1
|CLNDBN=Leber's optic atrophy
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1174:NBK1224:C0917796:535000:104:58610003
|CLNHGVS=NC_012920.1:m.4917A>G
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=516001.0001
|COMMON=1
|Disease=Leber's optic atrophy
|FwdALT=G
|FwdREF=A
|REF=A
|RSPOS=4917
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;VLD;G5A;G5;HD;GNO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000170502110100
|WGT=0
|dbSNPBuildID=125
|rsid=28357980
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}