{{Rsnum
|rsid=61750172
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GUCY2D
|position=8014700
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GUCY2D
}}{{omim
|id=600179
|rsnum=61750172
|variant=0006
}}
{{omim
|id=600179
|rsnum=61750172
|variant=0007
}}{{ClinVar
|rsid=61750172
|Reversed=0
|FwdREF=C
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=7918018
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=GUCY2D:3000
|GENE_NAME=GUCY2D
|GENE_ID=3000
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000017.10:g.7918018C>A; NC_000017.10:g.7918018C>T
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=600179.0005; RISN-GC1:c.2512C>A; 600179.0006; 600179.0007; RISN-GC1:c.2512C>T
|CLNSIG=5
|CLNCUI=C1866293; C1866293
|CLNDBN=Cone-rod dystrophy 6; not provided
|Disease=Cone-rod dystrophy 6; not provided
|CLNACC=RCV000009948.3; RCV000084861.1; RCV000009949.1; RCV000009950.1; RCV000084862.1
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1866293:601777:1872
}}