RS113994203 PAFAH1B1

Health Risk Chr 17:2676606 snv splice donor variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Lissencephaly due to LIS1 mutation
Lissencephaly due to LIS1 mutation
Population Frequencies
gnomAD ALL
0%
Other Variants in PAFAH1B1
rs121434482 rs121434483 rs1567561137 rs121434484 rs121434485 rs121434486 rs121434487 rs121434488 rs121434489 rs121434490
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