{{Rsnum
|rsid=7764472
|Gene=TULP1
|Chromosome=6
|position=35511797
|Orientation=plus
|GMAF=0.1129
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=TULP1
}}{{Venter SNP
|rsid=7764472
|allele=C
|frequency=
|uid=1103652839707
|type=homozygous_SNP
|hugo=TULP1
|ensembl gene=ENSG00000112041
|ensembl transcript=ENST00000229771
|sift=TOLERATED
|disease=Defects in TULP1 are the cause of retinitis pigmentosa type 14 (RP14) (MIM:600132); an autosomal recessive form of vision defect.
}}

{{ClinVar
|rsid=7764472
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=35479574
|CHROM=6
|GMAF=0.1126
|dbSNPBuildID=116
|SSR=0
|SAO=0
|VP=050168000a0505051e100100
|GENEINFO=TULP1:7287
|GENE_NAME=TULP1
|GENE_ID=7287
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.35479574G>C
|CLNSIG=1
|Tags=PM;PMC;SLO;NSM;REF;ASP;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;LSD
}}

{{PMID Auto
|PMID=19339744
|Title=Genetic analysis of Indian families with autosomal recessive retinitis pigmentosa by homozygosity screening.
|OA=1
}}

{{GET Evidence
|gene=TULP1
|aa_change=Thr67Arg
|aa_change_short=T67R
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7764472
|overall_frequency_n=9311
|overall_frequency_d=10288
|overall_frequency=0.905035
|n_genomes=48
|n_genomes_annotated=0
|n_haplomes=90
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=3
|autoscore=3
|n_web_uneval=1
}}

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