RS878853243 TSPAN12

Health Risk Chr 7:120806619
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What This Variant Does
"CLNSIG=5
Associated Conditions
Atrophia bulborum hereditaria
Exudative vitreoretinopathy 5
Persistent hyperplastic primary vitreous
autosomal recessive
Familial exudative vitreoretinopathy
Atrophia bulborum hereditaria
Exudative vitreoretinopathy 5
Persistent hyperplastic primary vitreous
autosomal recessive
Familial exudative vitreoretinopathy
Other Variants in TSPAN12
rs267607154 rs1554403626 rs267607153 rs794726655 rs267607152 rs587777283 rs587777284 rs538591733 rs587777285 rs759104377
Ask Dr. Hemsworth about this variant