{{Rsnum
|rsid=104886303
|Chromosome=X
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=COL4A5
|position=108695409
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=COL4A5
}}{{omim
|id=303630
|rsnum=104886303
|variant=0014
}}{{ClinVar
|rsid=104886303
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=107938639
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=COL4A5:1287
|GENE_NAME=COL4A5
|GENE_ID=1287
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.107938639T>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1207; 303630.0014
|CLNSIG=5
|CLNCUI=C1567742; C1567741
|CLNDBN=Alport syndrome, X-linked recessive
|Disease=Alport syndrome
|CLNACC=RCV000011212.4
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1207:C1567742:301050:63:88917
}}{{PMID Auto
|PMID=8651292
|Title=A mutation causing Alport syndrome with tardive hearing loss is common in the western United States.
|OA=1
}}