{{Rsnum
|rsid=121909536
|Gene=ANG
|Chromosome=14
|position=20693686
|Orientation=plus
|GMAF=0.0004591
|Gene_s=ANG,RNASE4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{omim
|id=105850
|rsnum=121909536
|variant=0002
}}{{ClinVar
|rsid=121909536
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=21161845
|CHROM=14
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|GENEINFO=RNASE4:6038; ANG:283
|GENE_NAME=RNASE4; ANG
|GENE_ID=6038; 283
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.21161845A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=105850.0002
|CLNSIG=5
|CLNCUI=C2678468
|CLNDBN=Amyotrophic lateral sclerosis type 9
|Disease=Amyotrophic lateral sclerosis type 9
|CLNACC=RCV000019700.26
|Tags=PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1450:C2678468:611895:803
|COMMON=0
}}