{{Rsnum
|rsid=104886043
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=COL4A5
|position=108559083
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=COL4A5
}}{{omim
|id=303630
|rsnum=104886043
|variant=0013
}}{{ClinVar
|rsid=104886043
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=107802313
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=COL4A5:1287
|GENE_NAME=COL4A5
|GENE_ID=1287
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.107802313G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=303630.0013
|CLNSIG=5
|CLNCUI=C1567742; C1567741; C0345893
|CLNDBN=Alport syndrome, X-linked recessive
|Disease=Alport syndrome
|CLNACC=RCV000011211.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1207:C1567742:301050:63:88917
}}{{PMID Auto
|PMID=8825605
|Title=A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome.
}}