{{Rsnum
|rsid=191205969
|Gene=TRPM1
|Chromosome=15
|position=31068010
|Orientation=plus
|GMAF=0.0009183
|Gene_s=TRPM1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|ALT=G
|CAF=0.9991; 0.0009183
|CHROM=15
|CLNACC=RCV000006605.1
|CLNALLE=1
|CLNDBN=Congenital stationary night blindness, type 1C
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2750747:613216:215
|CLNHGVS=NC_000015.9:g.31360213A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603576.0005
|COMMON=1
|Disease=Congenital stationary night blindness
|FwdALT=G
|FwdREF=A
|GENEINFO=TRPM1:4308
|GENE_ID=4308
|GENE_NAME=TRPM1
|REF=A
|RSPOS=31360213
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000016110100
|WGT=0
|dbSNPBuildID=135
|rsid=191205969
}}