RS1057520918 CACNA1A

Health Risk Chr 19:13262780
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Developmental and epileptic encephalopathy
42
Episodic ataxia type 2
Spinocerebellar ataxia type 6
Migraine
familial hemiplegic
1
52
Inborn genetic diseases
Developmental and epileptic encephalopathy
42
Episodic ataxia type 2
Spinocerebellar ataxia type 6
Migraine
Other Variants in CACNA1A
rs121908211 rs121908212 rs121908213 rs121908214 rs587776692 rs587776693 rs121908216 rs121908215 rs121908218 rs121908233
Ask Dr. Hemsworth about this variant