{{Rsnum
|rsid=104886432
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=COL4A5
|position=108575910
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=COL4A5
}}{{ClinVar
|ALT=GC,GG
|CHROM=X
|CLNACC=RCV000021166.1
|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.107819140dupG
|CLNSIG=5
|Disease=Alport syndrome
|FwdALT=GC,GG
|FwdREF=G
|REF=G
|RSPOS=107819140
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=132
|rsid=104886432
}}{{PMID Auto
|PMID=11462238
|Title=Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome.
}}