{{Rsnum
|rsid=36026860
|Gene=SEMA3A
|Chromosome=7
|position=84005501
|Orientation=minus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=SEMA3A
}}{{PMID Auto
|PMID=19957197
|Title=Candidate gene analysis of semaphorins in patients with Alzheimer's disease
}}{{ClinVar
|ALT=C
|CAF=0.9991; 0.0009183
|CHROM=7
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.83634817T>C
|CLNSIG=1
|COMMON=0
|FwdALT=G
|FwdREF=A
|GENEINFO=SEMA3A:10371
|GENE_ID=10371
|GENE_NAME=SEMA3A
|REF=T
|RSPOS=83634817
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;VLD;GNO;KGPhase1;KGPROD;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000040116100100
|WGT=0
|dbSNPBuildID=126
|rsid=36026860
|CLNACC=RCV000059787.1
|CLNDBN=not provided
|CLNSRC=UniProtKB (variants)
|CLNSRCID=VAR_069202
|Disease=not provided
}}{{PMID Auto
|PMID=22927827
|Title=SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.
|OA=1
}}