List of variants in gene ARX reported as benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_139058.3(ARX):c.1073+191C>T	rs73473563	0.14834
NM_139058.3(ARX):c.1073+225C>T	rs73207283	0.09240
NM_139058.3(ARX):c.1347C>T (p.Gly449=)	rs75489697	0.01993
NM_139058.3(ARX):c.-83C>A	rs751531684	0.00114
NM_139058.3(ARX):c.1599C>G (p.Ala533=)	rs1057523196	0.00012
NM_139058.3(ARX):c.1120-157C>G	rs192363904
NM_139058.3(ARX):c.1296C>T (p.Ala432=)	rs990653917
NM_139058.3(ARX):c.1300GCC[9] (p.Ala439_Ala440dup)	rs398124508
NM_139058.3(ARX):c.1448+161dup	rs375420492

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