RS886041999 CAMTA1

Health Risk Chr 1:7663429
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What This Variant Does
"CLNSIG=5
Associated Conditions
Cerebellar dysfunction with variable cognitive and behavioral abnormalities
Inborn genetic diseases
Cerebellar dysfunction with variable cognitive and behavioral abnormalities
Inborn genetic diseases
Other Variants in CAMTA1
rs374177752 rs863224853 rs886041635 rs886043243 rs1057524775 rs1057523792 rs1064796146 rs1064795180 rs1553239242 rs1085307743
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