{{Rsnum
|rsid=104886293
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=COL4A5
|position=108692850
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,C
|CHROM=X
|CLNACC=RCV000021630.3
|CLNALLE=2
|CLNDBN=Alport syndrome, X-linked recessive
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1207:C1567742:301050:63:88917
|CLNHGVS=NC_000023.10:g.107936080G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=303630.0009
|Disease=Alport syndrome
|FwdALT=A,C
|FwdREF=G
|GENEINFO=COL4A5:1287
|GENE_ID=1287
|GENE_NAME=COL4A5
|REF=G
|RSPOS=107936080
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050268000000000002110100
|WGT=0
|dbSNPBuildID=132
|rsid=104886293
}}{{PMID Auto
|PMID=9195222
|Title=The clinical spectrum of type IV collagen mutations.
}}