RS1977089420 SEMA6B

Health Risk Chr 19:4543896
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Associated Conditions
Epilepsy
progressive myoclonic
11
Inborn genetic diseases
Epilepsy
progressive myoclonic
11
Inborn genetic diseases
Other Variants in SEMA6B
rs2145342438 rs2512182702 rs142864702 rs2512182831 rs2512183344 rs1418798663 rs2512182790 rs2512182865 rs373413237 rs2145347825
Ask Dr. Hemsworth about this variant