{{Rsnum
|rsid=121909539
|Chromosome=14
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ANG
|position=20693753
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ANG,RNASE4
}}{{omim
|id=105850
|rsnum=121909539
|variant=0005
}}{{ClinVar
|rsid=121909539
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=21161912
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RNASE4:6038; ANG:283
|GENE_NAME=RNASE4; ANG
|GENE_ID=6038; 283
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.21161912C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=105850.0005
|CLNSIG=5
|CLNCUI=C2678468
|CLNDBN=Amyotrophic lateral sclerosis type 9
|Disease=Amyotrophic lateral sclerosis type 9
|CLNACC=RCV000019703.26
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1450:C2678468:611895:803
}}