List of variants reported as benign for dystonia 5

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Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_000161.3(GCH1):c.-121T>C	rs1753589	0.96017
NM_000161.3(GCH1):c.*243C>T	rs841	0.22091
NM_000161.3(GCH1):c.*732A>G	rs45454691	0.10500
NM_000161.3(GCH1):c.*1230C>T	rs56130647	0.07553
NM_000161.3(GCH1):c.-40C>T	rs28458175	0.05363
NM_000161.3(GCH1):c.*1183C>T	rs76009965	0.05289
NM_000161.3(GCH1):c.-131C>T	rs115939621	0.04950
NM_000161.3(GCH1):c.*1142G>A	rs10151500	0.04130
NM_000161.3(GCH1):c.*1915T>C	rs17128017	0.01571
NM_000161.3(GCH1):c.509+15G>A	rs116688703	0.00856
NM_000161.3(GCH1):c.-69G>C	rs533157442	0.00580
NM_000161.3(GCH1):c.68C>T (p.Pro23Leu)	rs41298432	0.00389
NM_000161.3(GCH1):c.*93G>A	rs41298438	0.00249
NM_000161.3(GCH1):c.211C>T (p.Leu71=)	rs141883031	0.00227
NM_000161.3(GCH1):c.*736A>G	rs150176097	0.00151
NM_000161.3(GCH1):c.*1044G>A	rs143961472	0.00088
NM_000161.3(GCH1):c.*12T>C	rs190993883	0.00057
NM_000161.3(GCH1):c.*1130C>G	rs543818323	0.00031
NM_000161.3(GCH1):c.507G>A (p.Ala169=)	rs150158277	0.00029
NM_000161.3(GCH1):c.69C>T (p.Pro23=)	rs767294964	0.00023
NM_000161.3(GCH1):c.*256A>G	rs181674470	0.00014
NM_000161.3(GCH1):c.582G>A (p.Thr194=)	rs199836777	0.00006
NM_000161.3(GCH1):c.*1010C>T	rs764569623	0.00004
NM_000161.3(GCH1):c.509+8T>A	rs753570450	0.00003
NM_000161.3(GCH1):c.542-19C>T	rs201405174	0.00003
NC_000014.9:g.54902903_54902920del	rs1408430070
NM_000161.3(GCH1):c.*1122A>T	rs56126158
NM_000161.3(GCH1):c.*1176C>G	rs113211390
NM_000161.3(GCH1):c.*677G>A	rs10136966
NM_000161.3(GCH1):c.*727A>G	rs138578359
NM_000161.3(GCH1):c.*830A>T	rs542811477
NM_000161.3(GCH1):c.344-16715G>A	rs11158026
NM_000161.3(GCH1):c.626+9G>T	rs374007793

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