{{Rsnum
|rsid=267606745
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=COL4A3
|position=227295044
|Gene_s=COL4A3,PAPPA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=2
|CLNACC=RCV000019044.26
|CLNALLE=1
|CLNDBN=Alport syndrome, autosomal dominant
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1207:C1567743:104200:63:88918
|CLNHGVS=NC_000002.11:g.228159760G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=120070.0010
|Disease=Alport syndrome
|FwdALT=A
|FwdREF=G
|GENEINFO=COL4A3:1285; AC097662.2:654841
|GENE_ID=1285; 654841
|GENE_NAME=COL4A3; AC097662.2
|REF=G
|RSPOS=228159760
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606745
}}