{{Rsnum
|rsid=104886270
|Gene=COL4A5
|Chromosome=X
|position=108686060
|Orientation=plus
|GMAF=0.0
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ClinVar
|rsid=104886270
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=107929290
|CHROM=X
|GMAF=0
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050068000000000016110100
|GENEINFO=COL4A5:1287
|GENE_NAME=COL4A5
|GENE_ID=1287
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.107929290C>T
|CLNSRC=ARUP_COL4A5
|CLNSIG=5
|CLNCUI=C1567741
|CLNDBN=Alport syndrome, X-linked recessive
|Disease=Alport syndrome
|CLNACC=RCV000021597.1
|Tags=PM;PMC;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=1; 0
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1207:C1567742:301050:63:88917
|COMMON=0
}}{{PMID Auto
|PMID=8651296
|Title=X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene.
|OA=1
}}
{{omim
|id=301050
|rsnum=104886270
}}