List of variants reported as benign for Stromme syndrome

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Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_016343.4(CENPF):c.8827A>G (p.Arg2943Gly)	rs438034	0.51075
NM_016343.4(CENPF):c.8186G>A (p.Arg2729Gln)	rs335524	0.45125
NM_016343.4(CENPF):c.33G>A (p.Gly11=)	rs2070064	0.36558
NM_016343.4(CENPF):c.2890C>T (p.Leu964=)	rs3795521	0.36312
NM_016343.4(CENPF):c.7186A>G (p.Asn2396Asp)	rs3748697	0.36093
NM_016343.4(CENPF):c.1482C>G (p.His494Gln)	rs2070065	0.25415
NM_016343.4(CENPF):c.4543G>A (p.Ala1515Thr)	rs2666839	0.25028
NM_016343.4(CENPF):c.5310T>A (p.His1770Gln)	rs3748693	0.20011
NM_016343.4(CENPF):c.3097G>A (p.Gly1033Arg)	rs3795518	0.10931
NM_016343.4(CENPF):c.1806A>G (p.Leu602=)	rs2070066	0.10927
NM_016343.4(CENPF):c.6032A>C (p.Glu2011Ala)	rs3790647	0.07578
NM_016343.4(CENPF):c.5933A>G (p.Asp1978Gly)	rs3790646	0.07439
NM_016343.4(CENPF):c.5302G>A (p.Asp1768Asn)	rs3748692	0.07434
NM_016343.4(CENPF):c.7386A>G (p.Glu2462=)	rs3748698	0.07416
NM_016343.4(CENPF):c.7067C>T (p.Ala2356Val)	rs3748696	0.07410
NM_016343.4(CENPF):c.2260C>G (p.Gln754Glu)	rs3795523	0.07179
NM_016343.4(CENPF):c.4461T>G (p.Leu1487=)	rs3795516	0.07164
NM_016343.4(CENPF):c.7581G>A (p.Leu2527=)	rs3790648	0.07113
NM_016343.4(CENPF):c.7611T>C (p.Leu2537=)	rs3790649	0.07111
NM_016343.4(CENPF):c.6415G>A (p.Ala2139Thr)	rs3748695	0.07107
NM_016343.4(CENPF):c.6674A>G (p.Gln2225Arg)	rs12058704	0.07101
NM_016343.4(CENPF):c.3314C>T (p.Thr1105Ile)	rs12067133	0.06848
NM_016343.4(CENPF):c.3052T>G (p.Tyr1018Asp)	rs3795519	0.06847
NM_016343.4(CENPF):c.4235T>C (p.Leu1412Ser)	rs3795517	0.06844
NM_016343.4(CENPF):c.6131C>T (p.Ser2044Leu)	rs7533166	0.03766
NM_016343.4(CENPF):c.3244C>T (p.His1082Tyr)	rs61732031	0.01115
NM_016343.4(CENPF):c.5635C>T (p.Arg1879Cys)	rs61732022	0.01110
NM_016343.4(CENPF):c.2101A>G (p.Met701Val)	rs3795524
NM_016343.4(CENPF):c.2444G>A (p.Arg815His)	rs3795522
NM_016343.4(CENPF):c.9318C>G (p.Asn3106Lys)	rs7289

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