C3888093[trait identifier] AND "Biochemical Molecular Genetic Laborato - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 800984	NM_001139.3(ALOX12B):c.1958T>G (p.Phe653Cys)	ALOX12B (F653C)	Single nucleotide variant (missense variant)	Autosomal recessive congenital ichthyosis 2	GUncertain significance
Select item 992981	NM_001139.3(ALOX12B):c.830T>A (p.Ile277Asn)	ALOX12B, LOC130060196 (I277N)	Single nucleotide variant (missense variant)	Autosomal recessive congenital ichthyosis 2	GUncertain significance