{{Rsnum
|rsid=267607034
|Chromosome=1
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=SEMA4A
|position=156163009
|Gene_s=SEMA4A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=1
|CLNACC=RCV000003526.1; RCV000003527.1
|CLNALLE=1
|CLNDBN=Retinitis pigmentosa 35; Cone-rod dystrophy 10
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1417:C1853214:610282:ORPHA791; C1846529:610283:ORPHA1872
|CLNHGVS=NC_000001.11:g.156163009T>G
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_001193301.1:c.1049T>G; 607292.0002
|Disease=Retinitis pigmentosa 35; Cone-rod dystrophy 10
|FwdALT=G
|FwdREF=T
|GENEINFO=SEMA4A:64218
|GENE_ID=64218
|GENE_NAME=SEMA4A
|REF=T
|RSPOS=156163009
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=267607034
|CLNORIGIN=1
}}