List of variants in gene TSPEAR reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 98; Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis; Tooth agenesis, selective, 10

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_144991.3(TSPEAR):c.1877T>C (p.Phe626Ser)	rs369010851	0.00011
NM_144991.3(TSPEAR):c.1336+5G>A
NM_144991.3(TSPEAR):c.1882G>A (p.Ala628Thr)

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