{{Rsnum
|rsid=76857106
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RNASEH2A
|position=12806782
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RNASEH2A
}}{{omim
|id=606034
|rsnum=76857106
|variant=0001
}}{{ClinVar
|rsid=76857106
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=12917596
|CHROM=19
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=RNASEH2A:10535
|GENE_NAME=RNASEH2A
|GENE_ID=10535
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.12917596G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=606034.0001
|CLNSIG=5
|CLNCUI=C1835912
|CLNDBN=Aicardi Goutieres syndrome 4
|Disease=Aicardi Goutieres syndrome 4
|CLNACC=RCV000004904.2
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1475:C1835912:610333:51
}}{{PMID|16845400}} Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutieres syndrome and mimic congenital viral brain infection.