List of variants reported as benign for Autosomal recessive DOPA responsive dystonia by Invitae

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Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NC_000011.10:g.2172367C>T	rs10770140	0.58545
NC_000011.10:g.2172610A>G	rs10770141	0.56453
NM_000360.4(TH):c.1334+127T>C	rs2070762	0.42406
NM_000360.4(TH):c.241G>A (p.Val81Met)	rs6356	0.31555
NM_000360.4(TH):c.977+8C>G	rs12419447	0.27597
NM_000360.4(TH):c.720G>A (p.Lys240=)	rs6357	0.23916
NM_000360.4(TH):c.312+289G>C	rs7482510	0.17720
NM_000360.4(TH):c.210T>C (p.Ala70=)	rs7950050	0.03941
NM_000360.4(TH):c.186G>A (p.Ser62=)	rs34510659	0.02696
NM_000360.4(TH):c.1401C>T (p.Asp467=)	rs3842724	0.02616
NM_000360.4(TH):c.1035G>T (p.Ala345=)	rs11826260	0.01611
NM_000360.4(TH):c.1278G>A (p.Thr426=)	rs36097848	0.01234
NM_000360.4(TH):c.1200+9C>T	rs11564717	0.01045
NM_000360.4(TH):c.487+3G>A	rs11042950	0.00795
NM_000360.4(TH):c.684G>A (p.Glu228=)	rs11564716	0.00706
NM_000360.4(TH):c.579C>T (p.Gly193=)	rs147852210	0.00547
NM_000360.4(TH):c.16G>A (p.Ala6Thr)	rs74555599	0.00462
NM_000360.4(TH):c.267G>A (p.Arg89=)	rs76240471	0.00359
NM_000360.4(TH):c.1105-14C>T	rs200496790	0.00101
NM_000360.4(TH):c.627C>G (p.Ile209Met)	rs202149985	0.00027
NM_000360.4(TH):c.1368C>T (p.Ser456=)	rs45538536	0.00023
NM_000360.4(TH):c.1047+16G>A	rs372706117	0.00017
NM_000360.4(TH):c.679G>A (p.Glu227Lys)	rs536382000	0.00017
NM_000360.4(TH):c.576+13C>T	rs369163325	0.00016
NM_000360.4(TH):c.51C>T (p.Ala17=)	rs199645400	0.00009
NM_000360.4(TH):c.252G>A (p.Leu84=)	rs758016812	0.00007
NM_000360.4(TH):c.264G>A (p.Pro88=)	rs113140700	0.00004
NM_000360.4(TH):c.313-9C>T	rs538345855	0.00004
NM_000360.4(TH):c.66C>T (p.Asp22=)	rs377073512	0.00003
NM_000360.4(TH):c.576+16dup	rs1238963534
NM_000360.4(TH):c.644+15C>A	rs191712999
NM_000360.4(TH):c.644+15C>T	rs191712999
NM_000360.4(TH):c.644+8dup

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