{{Rsnum
|rsid=75146158
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=RNASEH2C
|position=65720085
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KAT5,RNASEH2C
}}{{omim
|id=610330
|rsnum=75146158
|variant=0002
}}{{ClinVar
|rsid=75146158
|Reversed=1
|FwdREF=A
|FwdALT=T
|REF=T
|ALT=A
|RSPOS=65487556
|CHROM=11
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=RNASEH2C:84153; KAT5:10524
|GENE_NAME=RNASEH2C; KAT5
|GENE_ID=84153; 10524
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.65487556T>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=610330.0002
|CLNSIG=5
|CLNCUI=C1835916
|CLNDBN=Aicardi Goutieres syndrome 3
|Disease=Aicardi Goutieres syndrome 3
|CLNACC=RCV000001323.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1475:C1835916:610329:51
}}{{PMID Auto
|PMID=16845400
|Title=Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutieres syndrome and mimic congenital viral brain infection.
}}