ClinVar (all) for Orgtrack (Select 509431) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2920607	NM_001044.5(SLC6A3):c.950_989del	SLC6A3	Deletion (3 prime UTR variant)	Schizophrenia	GUncertain risk allele
Select item 2920606	NM_001044.5(SLC6A3):c.419-3595A>T	SLC6A3	Single nucleotide variant (intron variant)	Schizophrenia	GBenign
Select item 2920605	NC_000005.10:g.1448033A>G	SLC6A3	Single nucleotide variant	Schizophrenia	GBenign
Select item 1164244	NC_000011.10:g.2172610A>G	TH	Single nucleotide variant (genic upstream transcript variant)	Schizophrenia +1 more	GBenign
Select item 256814	NM_000795.4(DRD2):c.939T>C (p.His313=)	DRD2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 21866	NM_000360.4(TH):c.241G>A (p.Val81Met)	TH (V112M +2 more)	Single nucleotide variant (missense variant)	Autosomal recessive DOPA responsive dystonia +3 more	GBenign/Likely benign
Select item 17591	NM_000754.4(COMT):c.472G>A (p.Val158Met)	COMT (V158M +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 2105	NM_178510.2(ANKK1):c.2137G>A (p.Glu713Lys)	ANKK1 (E713K)	Single nucleotide variant (missense variant)	Schizophrenia +2 more	GBenign

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