List of variants reported as likely benign for Waardenburg syndrome type 2A

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001122659.3(EDNRB):c.914G>A (p.Ser305Asn)	rs5352	0.01109
NM_001354604.2(MITF):c.*1941A>G	rs192503700	0.00100
NM_001354604.2(MITF):c.355-1113C>T	rs199515469	0.00041
NM_001354604.2(MITF):c.*12T>C	rs201375960	0.00012
NM_001354604.2(MITF):c.1154A>G (p.Asn385Ser)	rs368915509	0.00008
NM_001354604.2(MITF):c.1180-11T>C	rs538450872	0.00002
NM_001354604.2(MITF):c.1222C>G (p.Pro408Ala)	rs199992377	0.00002
NM_001354604.2(MITF):c.1056C>T (p.Thr352=)	rs766006413	0.00001
NM_001354604.2(MITF):c.1064A>G (p.Lys355Arg)	rs751147980	0.00001
NM_001354604.2(MITF):c.669G>A (p.Met223Ile)	rs1032758072

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