List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 21 by 3billion

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_005422.4(TECTA):c.248C>T (p.Thr83Met)	rs145898158	0.00009
NM_005422.4(TECTA):c.2409G>A (p.Ser803=)	rs778543447	0.00001
NM_005422.4(TECTA):c.3769G>A (p.Gly1257Ser)	rs727504469	0.00001
NM_005422.4(TECTA):c.5741C>G (p.Pro1914Arg)

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