| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Copy number gain | not specified | |
| | | Copy number gain | not specified | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Microsatellite (intron variant) | not specified | |
| | | Microsatellite (intron variant) | not specified | |
| | | Microsatellite (intron variant) | not specified | |
| | | Microsatellite (intron variant) | not specified | |
| | | Microsatellite (intron variant) | not specified | |
| | | Indel (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Microsatellite (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Deletion (splice donor variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Copy number gain | Chromosome 1q21.1 duplication syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Duplication | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Duplication (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | RORC-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Deletion (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | |