List of variants reported as benign for Developmental and epileptic encephalopathy, 1; Intellectual disability, X-linked, with or without seizures, arx-related

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Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_139058.3(ARX):c.1347C>T (p.Gly449=)	rs75489697	0.01993
NM_139058.3(ARX):c.1671G>A (p.Thr557=)	rs190910161	0.00349
NM_139058.3(ARX):c.1074-3T>C	rs200700643	0.00337
NM_139058.3(ARX):c.802G>T (p.Val268Leu)	rs587783141	0.00093
NM_139058.3(ARX):c.1247C>G (p.Ala416Gly)	rs778734352	0.00023
NM_139058.3(ARX):c.663C>T (p.Thr221=)	rs1006404746	0.00017
NM_139058.3(ARX):c.1119+6C>T	rs201300786	0.00015
NM_139058.3(ARX):c.148T>C (p.Leu50=)	rs370342380	0.00015
NM_139058.3(ARX):c.223T>G (p.Phe75Val)	rs999545482	0.00005
NM_139058.3(ARX):c.99G>A (p.Leu33=)	rs756804509	0.00004
NM_139058.3(ARX):c.1524G>A (p.Val508=)	rs1056460685	0.00002
NM_139058.3(ARX):c.300G>A (p.Ala100=)	rs797045294	0.00002
NM_139058.3(ARX):c.361C>A (p.Pro121Thr)	rs1308958274	0.00002
NM_139058.3(ARX):c.1521C>A (p.Ala507=)	rs777179729	0.00001
NM_139058.3(ARX):c.738C>T (p.Asp246=)	rs750465338	0.00001
NM_139058.3(ARX):c.1073+20G>A
NM_139058.3(ARX):c.1186C>A (p.Pro396Thr)	rs776523818
NM_139058.3(ARX):c.1272G>T (p.Pro424=)	rs398124507
NM_139058.3(ARX):c.1300GCC[8] (p.Ala440dup)	rs398124508
NM_139058.3(ARX):c.1333C>T (p.Pro445Ser)	rs2147320407
NM_139058.3(ARX):c.1345G>A (p.Gly449Ser)	rs2147320401
NM_139058.3(ARX):c.215G>C (p.Ser72Thr)	rs1556056580
NM_139058.3(ARX):c.306GGC[8] (p.Ala114_Ala115del)	rs387906492
NM_139058.3(ARX):c.306GGC[9] (p.Ala115del)	rs387906492
NM_139058.3(ARX):c.421G>A (p.Gly141Ser)	rs2048712606
NM_139058.3(ARX):c.433G>T (p.Ala145Ser)	rs1438576250
NM_139058.3(ARX):c.441_455del (p.Ala151_Ala155del)	rs750585274
NM_139058.3(ARX):c.441_464del (p.Ala148_Ala155del)	rs398124510

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