List of variants reported as benign for amyotrophic lateral sclerosis type 12

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Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_001008212.2(OPTN):c.553-5C>T	rs2244380	0.80823
NM_021980.4(OPTN):c.-161T>C	rs71492279	0.36888
NM_001008212.2(OPTN):c.369+39T>G	rs79529484	0.22121
NM_001008212.2(OPTN):c.166+66A>G	rs10906303	0.20691
NM_001008212.2(OPTN):c.102G>A (p.Thr34=)	rs2234968	0.19474
NM_001008212.2(OPTN):c.-215G>A	rs11548142	0.18691
NM_001008212.2(OPTN):c.293T>A (p.Met98Lys)	rs11258194	0.05969
NM_001008212.2(OPTN):c.626+24G>A	rs11258211	0.03152
NM_001008212.2(OPTN):c.*269C>T	rs111484304	0.01294
NM_001008212.2(OPTN):c.-255C>G	rs2580915	0.01192
NM_001008212.2(OPTN):c.627-10T>C	rs80327830	0.00853
NM_001008212.2(OPTN):c.123G>A (p.Leu41=)	rs11591687	0.00729
NM_001008212.2(OPTN):c.964G>A (p.Glu322Lys)	rs523747	0.00719
NM_001008212.2(OPTN):c.963C>T (p.Ser321=)	rs150381274	0.00525
NM_001008212.2(OPTN):c.553-10G>A	rs11258210	0.00492
NM_001008212.2(OPTN):c.876G>A (p.Pro292=)	rs151065414	0.00118
NM_001008212.2(OPTN):c.1634G>A (p.Arg545Gln)	rs75654767	0.00101
NM_001008212.2(OPTN):c.779+20G>A	rs79733653	0.00095
NM_001008212.2(OPTN):c.1148+13A>G	rs368654623	0.00061
NM_001008212.2(OPTN):c.1612+10G>A	rs191671333	0.00053
NM_001008212.2(OPTN):c.147C>T (p.Thr49=)	rs187734249	0.00045
NM_001008212.2(OPTN):c.777A>T (p.Glu259Asp)	rs532842754	0.00035
NM_001008212.2(OPTN):c.-274C>A	rs552494483	0.00001
NM_001008212.2(OPTN):c.447G>A (p.Arg149=)	rs555741399	0.00001
NM_001008212.2(OPTN):c.1402-11del
NM_001008212.2(OPTN):c.1402-7C>T
NM_001008212.2(OPTN):c.402C>A (p.Ala134=)	rs113955718
NM_001008212.2(OPTN):c.964= (p.Glu322=)
NM_021980.4(OPTN):c.-227G>T	rs3814657

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