{{Rsnum
|rsid=113993970
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HTRA1
|position=122506817
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HTRA1
}}{{omim
|id=602194
|rsnum=113993970
|variant=0003
}}{{ClinVar
|rsid=113993970
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=124266333
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=HTRA1:5654
|GENE_NAME=HTRA1
|GENE_ID=5654
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.124266333C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK32533; 602194.0003
|CLNSIG=5
|CLNCUI=C1838577; C1838577
|CLNDBN=Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
|Disease=Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
|CLNACC=RCV000007917.2
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK32533:C1838577:600142:199354
}}