RS118203935 CYP4F22

Health Risk Chr 19:15549169 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive congenital ichthyosis 5
Lamellar ichthyosis
Autosomal recessive congenital ichthyosis 5
Lamellar ichthyosis
Population Frequencies
gnomAD ALL
100%
Other Variants in CYP4F22
rs118203936 rs118203937 rs531800013 rs146026019 rs202078702 rs150739429 rs371097842 rs148977089 rs374106918 rs199892192
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