{{Rsnum
|rsid=121918127
|Chromosome=9
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=INPP5E
|position=136429731
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=INPP5E
}}{{omim
|id=613037
|rsnum=121918127
|variant=0001
}}{{ClinVar
|rsid=121918127
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=139324183
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=INPP5E:56623
|GENE_NAME=INPP5E
|GENE_ID=56623
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.139324183G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=613037.0001
|CLNSIG=5
|CLNCUI=C1857802
|CLNDBN=MORM syndrome
|Disease=MORM syndrome
|CLNACC=RCV000000427.3
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1857802:610156
}}