"Mendelics"[submitter] AND "JMJD1C"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1685317	NM_032776.3(JMJD1C):c.7168C>G (p.Leu2390Val)	JMJD1C (L2102V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GBenign
Select item 1684818	NM_032776.3(JMJD1C):c.5309T>C (p.Ile1770Thr)	JMJD1C (I1482T +4 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 1684819	NM_032776.3(JMJD1C):c.4962A>T (p.Gln1654His)	JMJD1C (Q1366H +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1406536	NM_032776.3(JMJD1C):c.556C>T (p.Pro186Ser)	JMJD1C (P148S +2 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GConflicting classifications of pathogenicity

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