{{Rsnum
|rsid=121434559
|Chromosome=15
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SNX22
|position=64156802
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PPIB,SNX22
}}{{omim
|id=123841
|rsnum=121434559
|variant=0002
}}{{ClinVar
|rsid=121434559
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=64449001
|CHROM=15
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=SNX22:79856; PPIB:5479
|GENE_NAME=SNX22; PPIB
|GENE_ID=79856; 5479
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.64449001G>A
|CLNSRC=OMIM Allelic Variant; Osteogenesis Imperfecta Variant Database (PPIB)
|CLNORIGIN=1
|CLNSRCID=123841.0002; PPIB_00001
|CLNSIG=5
|CLNCUI=C1850169
|CLNDBN=Osteogenesis imperfecta type 9; not provided
|Disease=Osteogenesis imperfecta type 9; not provided
|CLNACC=RCV000018434.22; RCV000024534.1
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1850169:259440
}}