RS1042295993 RORC

Health Risk Chr 1:151815282
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Associated Conditions
Inborn genetic diseases
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
Other Variants in RORC
rs774357869 rs863225091 rs863225092 rs17582155 rs200303989 rs201691098 rs2101656625 rs1558164428 rs2525630257 rs1651702189
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