{{Rsnum
|rsid=121434405
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RPL5
|position=92833452
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FAM69A,RPL5
}}{{omim
|id=603634
|rsnum=121434405
|variant=0001
}}{{ClinVar
|rsid=121434405
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=92833452
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260080605000002110100
|GENEINFO=RPL5:6125; FAM69A:388650
|GENE_NAME=RPL5; FAM69A
|GENE_ID=6125; 388650
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.92833452C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000969.3:c.67C>T; NM_001252273.1:c.475-418G>A; 603634.0001
|CLNSIG=5
|CLNCUI=C0265265
|CLNDBN=Aase syndrome
|Disease=Aase syndrome
|CLNACC=RCV000006556.1
|Tags=PM;S3D;NSN;REF;INT;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK7047:C0265265:612561:ORPHA124:71988008
}}