RS1064796709 CACNA1A

Health Risk Chr 19:13212218
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What This Variant Does
"CLNSIG=4
Associated Conditions
Developmental and epileptic encephalopathy
42
Episodic ataxia type 2
Inborn genetic diseases
Developmental and epileptic encephalopathy
42
Episodic ataxia type 2
Inborn genetic diseases
Other Variants in CACNA1A
rs121908211 rs121908212 rs121908213 rs121908214 rs587776692 rs587776693 rs121908216 rs121908215 rs121908218 rs121908233
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