{{Rsnum
|rsid=113993969
|Chromosome=10
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HTRA1
|position=122506802
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HTRA1
}}{{omim
|id=602194
|rsnum=113993969
|variant=0004
}}{{ClinVar
|rsid=113993969
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=124266318
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HTRA1:5654
|GENE_NAME=HTRA1
|GENE_ID=5654
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.124266318G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=NBK32533; 602194.0004; VAR_063149
|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=RCV000007918.2
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK32533:C1838577:600142:199354
}}{{PMID Auto
|PMID=19387015
|Title=Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease.
}}