"Fulgent Genetics, Fulgent Genetics"[submitter] AND "PIRC66"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 316473	NM_000103.4(CYP19A1):c.953T>C (p.Met318Thr)	CYP19A1, MIR4713HG +1 more (M318T)	Single nucleotide variant (missense variant)	Aromatase deficiency +1 more	GUncertain significance
Select item 859794	NM_000103.4(CYP19A1):c.297-1G>C	CYP19A1, MIR4713HG +1 more	Single nucleotide variant (splice acceptor variant)	not provided +2 more	GLikely pathogenic