Related gene-specific medical variations for Gene (Select 57616) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685631	GRCh37/hg19 19q12(chr19:31760245-31850047)x1	TSHZ3	Copy number loss	not provided	GUncertain significance
Select item 980756	GRCh37/hg19 19q12(chr19:31051497-31804809)x3	TSHZ3	Copy number gain	not provided	GUncertain significance
Select item 980755	GRCh37/hg19 19q12(chr19:31532896-32341833)x1	TSHZ3	Copy number loss	not provided	GUncertain significance
Select item 635916	Single allele	TSHZ3	Duplication	Neurodevelopmental disorder	GUncertain significance
Select item 442189	GRCh37/hg19 19q12(chr19:31792864-32335982)x1	TSHZ3	Copy number loss	See cases	GUncertain significance
Select item 161739	NM_020856.4(TSHZ3):c.1181C>T (p.Ser394Leu)	TSHZ3 (S394L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

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