{{Rsnum
|rsid = 35445598
|Gene = RIMS1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=6
|position=72233802
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RIMS1
}}{{Venter SNP
|rsid=35445598
|allele=A
|frequency=
|uid=1103652900145
|type=heterozygous_SNP
|hugo=RIMS1
|ensembl gene=ENSG00000079841
|ensembl transcript=ENST00000264839
|sift=TOLERATED
|disease=Defects in RIMS1 are a cause of autosomal dominant cone- rod dystrophy (CORD7) (MIM:603649). CORD7 is characterized by early loss of visual acuity and color vision, followed by night blindness and peripheral visual field loss. The onset of reduced color vision and visual acuity varies between the ages of 20 and 40 years.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}