RS797045865 PAFAH1B1

Health Risk Chr 17:2674088
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What This Variant Does
"CLNSIG=5
Associated Conditions
Lissencephaly due to LIS1 mutation
Inborn genetic diseases
Lissencephaly due to LIS1 mutation
Inborn genetic diseases
Other Variants in PAFAH1B1
rs121434482 rs121434483 rs1567561137 rs121434484 rs121434485 rs121434486 rs121434487 rs121434488 rs121434489 rs121434490
Ask Dr. Hemsworth about this variant