"Mendelics"[submitter] AND "DISC1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1686626	NM_018662.3(DISC1):c.109C>T (p.Arg37Trp)	DISC1, TSNAX-DISC1 (R37W)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 1686627	NM_018662.3(DISC1):c.1453C>T (p.Gln485Ter)	DISC1, TSNAX-DISC1 (Q135* +2 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance