{{Rsnum
|rsid=2001030
|Gene=MT-RNR1
|Chromosome=MT
|position=1438
|Orientation=plus
|GMAF=0.04397
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 4.6 | 0.0 | 95.4
| HCB | 4.5 | 0.0 | 95.5
| JPT | 0.0 | 0.0 | 100.0
| YRI | 19.0 | 0.0 | 81.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 4.5 | 0.0 | 95.5
| 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=G1438A
|sources={{PMID|17099056}}
|tree=PhyloTree
|tree_build=7
|ancestral_haplogroup=H
|derived_haplogroup=H2
|ancestral_allele=G
|derived_allele=A
}}

{{ClinVar
|ALT=G
|CAF=0.04397; 0.956
|CHROM=MT
|CLNACC=RCV000035045.1
|CLNALLE=1
|CLNDBN=AllHighlyPenetrant
|CLNDSDB=MedGen
|CLNDSDBID=CN169374
|CLNHGVS=NC_012920.1:m.1438A>G
|CLNSIG=2
|COMMON=1
|Disease=AllHighlyPenetrant
|FwdALT=G
|FwdREF=A
|REF=A
|RSPOS=1438
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;SLO;VLD;G5;HD;GNO;OTHERKG;LSD
|VC=SNV
|VP=0x050160000000150502100100
|WGT=0
|dbSNPBuildID=92
|rsid=2001030
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}