RS371956016 MERTK

Health Risk Chr 2:112019523
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What This Variant Does
"CLNSIG=5
Associated Conditions
Retinitis pigmentosa 38
Inborn genetic diseases
Retinal dystrophy
Autosomal recessive retinitis pigmentosa
Retinitis pigmentosa
Clear cell carcinoma of kidney
Retinitis pigmentosa 38
Inborn genetic diseases
Retinal dystrophy
Autosomal recessive retinitis pigmentosa
Retinitis pigmentosa
Clear cell carcinoma of kidney
Other Variants in MERTK
rs730880273 rs119489105 rs1573554264 rs387907314 rs35898499 rs34072093 rs527236084 rs527236083 rs527236134 rs786205533
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