{{Rsnum
|rsid=104886438
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=COL4A5
|position=108578080
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=104886438
|Reversed=0
|FwdREF=A
|FwdALT=AG,AGG
|REF=A
|ALT=AG,AGG
|RSPOS=107821306
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050068000000000002110200
|GENEINFO=COL4A5:1287
|GENE_NAME=COL4A5
|GENE_ID=1287
|WGT=0
|VC=DIV
|CLNALLE=2; 1
|CLNSIG=5
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNACC=RCV000021187.1; RCV000021188.1
|CLNDBN=Alport syndrome, X-linked recessive
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1207:C1567742:301050:63:88917
|CLNHGVS=NC_000023.10:g.107821309_107821310dupGG; NC_000023.10:g.107821310dupG
|Disease=Alport syndrome
}}
{{omim
|id=301050
|rsnum=104886438
}}{{PMID Auto
|PMID=15954103
|Title=Novel COL4A5, COL4A4, and COL4A3 mutations in Alport syndrome.
}}