{{Rsnum
|rsid=41265017
|Gene=SEMA4A
|Chromosome=1
|position=156176849
|Orientation=plus
|GMAF=0.03076
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=SEMA4A
}}{{omim
|id=607292
|rsnum=41265017
|variant=0003
}}

{{GET Evidence
|gene=SEMA4A
|aa_change=Arg713Gln
|aa_change_short=R713Q
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs41265017
|overall_frequency_n=398
|overall_frequency_d=10758
|overall_frequency=0.0369957
|n_genomes=5
|n_genomes_annotated=0
|n_haplomes=6
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|in_omim=Y
|pph2_score=0.553
|genetests_testable=Y
|nblosum100=0
|autoscore=4
|webscore=N
|n_web_uneval=7
}}

{{ClinVar
|ALT=A
|CAF=0.9692; 0.03076
|CHROM=1
|CLNACC=RCV000003528.1
|CLNALLE=1
|CLNDBN=Retinitis pigmentosa 35
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1417:C1853214:610282:ORPHA791
|CLNHGVS=NC_000001.11:g.156176849G>A
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_001193301.1:c.2138G>A; 607292.0003
|COMMON=1
|Disease=Retinitis pigmentosa 35
|FwdALT=A
|FwdREF=G
|GENEINFO=SEMA4A:64218
|GENE_ID=64218
|GENE_NAME=SEMA4A
|REF=G
|RSPOS=156176849
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;NSM;REF;ASP;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a05150516110100
|WGT=1
|dbSNPBuildID=127
|rsid=41265017
|CLNORIGIN=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}