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{{omim |id=303630 |rsnum=104886303 |variant=0014 }}{{ClinVar |rsid=104886303 |Reversed=0 |FwdREF=T |FwdALT=G |REF=T |ALT=G |RSPOS=107938639 |CHROM=X |dbSNPBuildID=132 |SSR=0 |SAO=1 |VP=050268000a01000002110100 |GENEINFO=COL4A5:1287 |GENE_NAME=COL4A5 |GENE_ID=1287 |WGT=1 |VC=SNV |CLNALLE=1 |CLNHGVS=NC_000023.10:g.107938639T>G |CLNSRC=OMIM Allelic Variant; ARUP_COL4A5 |CLNORIGIN=1 |CLNSRCID=303630.0014; . |CLNSIG=5 |CLNCUI=C1567742; C1567741 |CLNDBN=Alport syndrome, X-linked recessive; Alport syndrome |Disease=Alport syndrome |CLNACC=SCV000031439.1; SCV000042326.1 |Tags=PM;PMC;S3D;NSM;REF;OTHERKG;LSD;OM }}{{PMID Auto |PMID=8651292 |Title=A mutation causing Alport syndrome with tardive hearing loss is common in the western United States. }}
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