{{Rsnum
|rsid=13297509
|Chromosome=9
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=INPP5E
|position=136431830
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=INPP5E
}}{{omim
|id=613037
|rsnum=13297509
|variant=0002
}}

{{ClinVar
|rsid=13297509
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=139326282
|CHROM=9
|dbSNPBuildID=121
|SSR=0
|SAO=1
|VP=0x050260000000000402110100
|GENEINFO=INPP5E:56623
|GENE_NAME=INPP5E
|GENE_ID=56623
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.139326282G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=613037.0002
|CLNSIG=5
|CLNCUI=CN119531
|CLNDBN=Joubert syndrome 1
|Disease=Joubert syndrome 1
|CLNACC=RCV000022402.1
|Tags=PM;S3D;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen
|CLNDSDBID=NBK1325:CN119531
}}

{{on chip | HumanOmni1Quad}}