NR2F1 Chromosome 5

Nuclear receptor subfamily 2 group F member 1
103 variants 103 Health Risk

Upload your DNA to see your personal genotypes for variants in NR2F1.

What This Gene Does
The protein encoded by this gene is a nuclear hormone receptor and transcriptional regulator. The encoded protein acts as a homodimer and binds to 5'-AGGTCA-3' repeats. Defects in this gene are a cause of Bosch-Boonstra optic atrophy syndrome (BBOAS). [provided by RefSeq, Apr 2014]
Gene Info
Gene Group
Nuclear receptor subfamily 2 group F
Locus Type
gene with protein product
Location
5q15
Ensembl
ENSG00000175745
Associated Conditions (8)
Inborn genetic diseases
Bosch-Boonstra-Schaaf optic atrophy syndrome
Epilepsy
Seizure
Neurodevelopmental delay
NR2F1-related disorder
Autism spectrum disorder
See cases
Key Variants
All Variants (103)
RSID Category Clinical Significance Conditions
RS1159055932 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1193147148 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1272746750 Health Risk Conflicting classifications of pathogenicity
RS1281166433 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1313433161 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1414612574 Health Risk Conflicting classifications of pathogenicity
RS1468965930 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1554074665 Health Risk Conflicting classifications of pathogenicity Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS1561523678 Health Risk Conflicting classifications of pathogenicity
RS1753203799 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1753205307 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1753213218 Health Risk Conflicting classifications of pathogenicity Bosch-Boonstra-Schaaf optic atrophy syndrome, Inborn genetic diseases, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS1753373048 Health Risk Conflicting classifications of pathogenicity Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS2149941603 Health Risk Conflicting classifications of pathogenicity Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS2149946003 Health Risk Conflicting classifications of pathogenicity Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS2480802060 Health Risk Conflicting classifications of pathogenicity Bosch-Boonstra-Schaaf optic atrophy syndrome, Epilepsy, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS2480802156 Health Risk Conflicting classifications of pathogenicity Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS2480802300 Health Risk Conflicting classifications of pathogenicity Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS2480808763 Health Risk Conflicting classifications of pathogenicity
RS370606773 Health Risk Conflicting classifications of pathogenicity
RS763566932 Health Risk Conflicting classifications of pathogenicity Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS954495672 Health Risk Conflicting classifications of pathogenicity
RS1057522318 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1064794459 Health Risk Likely pathogenic
RS1064797311 Health Risk Likely pathogenic Seizure, Seizure
RS1287146448 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS1554074682 Health Risk Likely pathogenic Neurodevelopmental delay, Neurodevelopmental delay
RS1554074684 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Inborn genetic diseases, Inborn genetic diseases
RS1554074850 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS1554075105 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS1561523716 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS1580358347 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS1580358677 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS1753211889 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS1753213365 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS1753260850 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS1753263819 Health Risk Likely pathogenic
RS1753264180 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1753268855 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS2149941524 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS2149941551 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS2149941577 Health Risk Likely pathogenic NR2F1-related disorder, NR2F1-related disorder
RS2149941610 Health Risk Likely pathogenic
RS2149941611 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS2149943169 Health Risk Likely pathogenic
RS2149943173 Health Risk Likely pathogenic
RS2149946049 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS2149946121 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
RS2480802211 Health Risk Likely pathogenic
RS2480802260 Health Risk Likely pathogenic Bosch-Boonstra-Schaaf optic atrophy syndrome, Bosch-Boonstra-Schaaf optic atrophy syndrome
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