{{Rsnum
|rsid=121434406
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RPL5
|position=92836283
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FAM69A,RPL5
}}{{omim
|id=603634
|rsnum=121434406
|variant=0002
}}{{ClinVar
|rsid=121434406
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=92836283
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x0502600a0a05000002110100
|GENEINFO=RPL5:6125; FAM69A:388650; SNORD21:6083
|GENE_NAME=RPL5; FAM69A; SNORD21
|GENE_ID=6125; 388650; 6083
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.92836283G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000969.3:c.418G>A; NM_001252273.1:c.475-3249C>T; NR_000006.8:n.-1006G>A; 603634.0002
|CLNSIG=5
|CLNCUI=C0265265
|CLNDBN=Aase syndrome
|Disease=Aase syndrome
|CLNACC=RCV000006557.1
|Tags=PM;S3D;NSM;REF;INT;R5;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK7047:C0265265:612561:ORPHA124:71988008
}}