RS786205529 SNRNP200

Health Risk Chr 2:96290475
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal dominant retinitis pigmentosa
Retinal dystrophy
Retinitis pigmentosa 33
Autosomal dominant retinitis pigmentosa
Retinal dystrophy
Retinitis pigmentosa 33
Other Variants in SNRNP200
rs267607077 rs397514574 rs397514575 rs375734152 rs527236115 rs527236113 rs527236114 rs368225080 rs376352502 rs377641548
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