{{Rsnum
|rsid=104886164
|Gene=COL4A5
|Chromosome=X
|position=108603032
|Orientation=plus
|GMAF=0.005441
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ClinVar
|ALT=G,T
|CAF=0.9946; 0.005441; .
|CHROM=X
|CLNACC=RCV000021375.1
|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.107846262C>T
|CLNSIG=5
|COMMON=1
|Disease=Alport syndrome
|FwdALT=G,T
|FwdREF=C
|GENEINFO=COL4A5:1287
|GENE_ID=1287
|GENE_NAME=COL4A5
|REF=C
|RSPOS=107846262
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000016110100
|WGT=0
|dbSNPBuildID=132
|rsid=104886164
}}{{PMID Auto
|PMID=10684360
|Title=Mutational analysis of COL4A5 gene in Korean Alport syndrome.
}}