RS775981553 UBE3B

Health Risk Chr 12:109483612
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Oculocerebrofacial syndrome
Kaufman type
Inborn genetic diseases
Oculocerebrofacial syndrome
Kaufman type
Other Variants in UBE3B
rs398123020 rs398123021 rs398123022 rs398123023 rs539407162 rs771222229 rs886041886 rs754032570 rs1555269815 rs753221661
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