List of variants in gene combination ARX, LOC109610631 reported as benign for X-linked disease

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: 8

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HGVS	dbSNP	gnomAD frequency
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.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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