List of variants reported as likely benign for Asphyxiating thoracic dystrophy 5; Nephronophthisis 13; Cranioectodermal dysplasia 4; Senior-Loken syndrome 8; Spermatogenic failure 72

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Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_025132.4(WDR19):c.1581C>A (p.Thr527=)	rs114689848	0.00847
NM_025132.4(WDR19):c.2142+12G>A	rs149621476	0.00246
NM_025132.4(WDR19):c.2363+7C>T	rs190180293	0.00066
NM_025132.4(WDR19):c.13+15G>A	rs150633358	0.00041
NM_025132.4(WDR19):c.1039C>T (p.Leu347=)	rs201958863	0.00027
NM_025132.4(WDR19):c.3435C>T (p.Ser1145=)	rs200659514	0.00014
NM_025132.4(WDR19):c.1797T>G (p.Ala599=)	rs373430338	0.00011
NM_025132.4(WDR19):c.99-11A>C	rs756899296	0.00009
NM_025132.4(WDR19):c.3261+20C>T	rs547317070	0.00007
NM_025132.4(WDR19):c.3358+14A>G	rs372822923	0.00007
NM_025132.4(WDR19):c.522+13C>T	rs374417243	0.00005
NM_025132.4(WDR19):c.962-11G>A	rs537505873	0.00005
NM_025132.4(WDR19):c.1962A>G (p.Ala654=)	rs770818331	0.00004
NM_025132.4(WDR19):c.2607C>T (p.Tyr869=)	rs371645967	0.00004
NM_025132.4(WDR19):c.2742T>C (p.Ala914=)	rs753812144	0.00004
NM_025132.4(WDR19):c.3716+13G>A	rs759523972	0.00003
NM_025132.4(WDR19):c.1357-8C>T	rs754713889	0.00002
NM_025132.4(WDR19):c.1752T>C (p.Tyr584=)	rs139391186	0.00002
NM_025132.4(WDR19):c.3624C>T (p.Asn1208=)	rs747334676	0.00002
NM_025132.4(WDR19):c.1350A>G (p.Leu450=)	rs770470368	0.00001
NM_025132.4(WDR19):c.2646-5T>C	rs771971475	0.00001
NM_025132.4(WDR19):c.2876+10T>C	rs773692164	0.00001
NM_025132.4(WDR19):c.2877-12A>G	rs754511582	0.00001
NM_025132.4(WDR19):c.42C>T (p.Gly14=)	rs531575276	0.00001
NM_025132.4(WDR19):c.1791T>C (p.Ile597=)	rs2109358310
NM_025132.4(WDR19):c.2364-4del	rs750106753
NM_025132.4(WDR19):c.2646-16G>T	rs750485530
NM_025132.4(WDR19):c.2876+10T>A	rs773692164
NM_025132.4(WDR19):c.3951T>C (p.Cys1317=)	rs564992065
NM_025132.4(WDR19):c.513G>T (p.Thr171=)	rs754543019
NM_025132.4(WDR19):c.6+6_6+8del	rs748952637

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