{{Rsnum
|rsid=121912863
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=COL4A4
|position=227008112
|Gene_s=COL4A4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=120131
|rsnum=121912863
|variant=0006
}}{{ClinVar
|rsid=121912863
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=227872828
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=COL4A4:1286
|GENE_NAME=COL4A4
|GENE_ID=1286
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.227872828G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=120131.0006
|CLNSIG=5
|CLNCUI=C1567744
|CLNDBN=Alport syndrome, autosomal recessive
|Disease=Alport syndrome
|CLNACC=RCV000018952.26
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1207:C1567744:203780:63:88919
}}