{{Rsnum
|rsid=137852869
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=NDUFA13
|position=19516253
|Gene_s=NDUFA13,TSSK6
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=609435
|variant=0001
|rsnum=137852869
}}{{ClinVar
|rsid=137852869
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=19627062
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=TSSK6:83983; NDUFA13:51079
|GENE_NAME=TSSK6; NDUFA13
|GENE_ID=83983; 51079
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.19627062G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609435.0001
|CLNSIG=5
|CLNCUI=C0749424
|CLNDBN=Hurthle cell carcinoma of thyroid
|Disease=Hurthle cell carcinoma of thyroid
|CLNACC=RCV000001761.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0749424:607464:146:423158009
}}