List of variants studied for autosomal recessive nonsyndromic hearing loss 91

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_004568.6(SERPINB6):c.431-25T>C	rs3818276	0.85848
NM_004568.6(SERPINB6):c.730-32G>A	rs318426	0.84542
NM_004568.6(SERPINB6):c.573+26A>G	rs2244693	0.63676
NM_004568.6(SERPINB6):c.54G>A (p.Thr18=)	rs2236277	0.29436
NM_004568.6(SERPINB6):c.268A>G (p.Met90Val)	rs2295769	0.22672
NM_004568.6(SERPINB6):c.121G>A (p.Val41Ile)	rs140220538	0.00057
NM_004568.6(SERPINB6):c.430+3G>A	rs201080069	0.00025
NM_004568.6(SERPINB6):c.1096G>A (p.Gly366Arg)	rs765798757	0.00006
NM_004568.6(SERPINB6):c.1022G>A (p.Arg341Gln)	rs760194824	0.00003
NM_004568.6(SERPINB6):c.203T>C (p.Ile68Thr)	rs1770382873	0.00001
NM_004568.6(SERPINB6):c.217C>T (p.Gln73Ter)
NM_004568.6(SERPINB6):c.251C>T (p.Thr84Met)	rs538616923
NM_004568.6(SERPINB6):c.3G>C (p.Met1Ile)	rs1225963332
NM_004568.6(SERPINB6):c.733G>T (p.Glu245Ter)	rs267607037

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