RS137853049 TUBA1A
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What This Variant Does
"[OMIM:?]
Associated Conditions
Lissencephaly due to TUBA1A mutation
Inborn genetic diseases
Tubulinopathy
Tubulinopathy-associated dysgyria
Lissencephaly due to TUBA1A mutation
Inborn genetic diseases
Tubulinopathy
Tubulinopathy-associated dysgyria
Other Variants in TUBA1A