List of variants in gene SMPX reported as uncertain significance for auditory system disorder

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_014332.3(SMPX):c.*395T>G	rs765339045	0.00035
NM_014332.3(SMPX):c.-103C>T	rs1301418010	0.00003
NM_014332.3(SMPX):c.*181A>G	rs2092772738
NM_014332.3(SMPX):c.*232T>G	rs1313352273
NM_014332.3(SMPX):c.*45A>T	rs1057515838
NM_014332.3(SMPX):c.-54G>A	rs1057515840
NM_014332.3(SMPX):c.238C>G (p.Leu80Val)	rs2147386996
NM_014332.3(SMPX):c.264G>A (p.Gln88=)	rs1057515839

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