RS387907136 CFAP418

Health Risk Chr 8:95247712
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What This Variant Does
"CLNSIG=5
Associated Conditions
Cone-rod dystrophy 16
Bardet-biedl syndrome 21
Retinitis pigmentosa
Autosomal recessive retinitis pigmentosa
Retinal dystrophy
Cone-rod dystrophy 16
Bardet-biedl syndrome 21
Retinitis pigmentosa
Autosomal recessive retinitis pigmentosa
Retinal dystrophy
Other Variants in CFAP418
rs1064792852 rs1064792853 rs387907137 rs148114532 rs115853053 rs35141355 rs150859301 rs143748636 rs1060505042 rs748014296
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