{{Rsnum
|rsid=121918302
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RIMS1
|position=72251007
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RIMS1
}}{{omim
|id=606629
|rsnum=121918302
|variant=0001
}}{{ClinVar
|rsid=121918302
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=72960710
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RIMS1:22999
|GENE_NAME=RIMS1
|GENE_ID=22999
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.72960710G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606629.0001
|CLNSIG=5
|CLNCUI=C1863634
|CLNDBN=Cone-rod dystrophy 7
|Disease=Cone-rod dystrophy 7
|CLNACC=RCV000004385.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1863634:603649:1872
}}