List of variants in gene combination INS, TH reported as benign for Autosomal recessive DOPA responsive dystonia

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000360.4(TH):c.1401C>T (p.Asp467=)	rs3842724	0.02616
NM_000360.4(TH):c.1278G>A (p.Thr426=)	rs36097848	0.01234
NM_000360.4(TH):c.1200+9C>T	rs11564717	0.01045

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