RS201691098 RORC

Health Risk Chr 1:151831727
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Associated Conditions
Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency
Inborn genetic diseases
Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency
Inborn genetic diseases
Other Variants in RORC
rs774357869 rs863225091 rs863225092 rs17582155 rs200303989 rs2101656625 rs1558164428 rs2525630257 rs1651702189 rs1042295993
Ask Dr. Hemsworth about this variant