List of variants reported as likely benign for Glaucoma of childhood by ClinGen Glaucoma Variant Curation Expert Panel

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000261.2(MYOC):c.1193A>G (p.Lys398Arg)	rs56314834	0.00406
NM_000261.2(MYOC):c.366C>T (p.Gly122=)	rs145354114	0.00244
NM_000261.2(MYOC):c.985G>A (p.Val329Met)	rs146391864	0.00086
NM_000261.2(MYOC):c.1058C>T (p.Thr353Ile)	rs137853277	0.00028
NM_000261.2(MYOC):c.136C>T (p.Arg46Ter)	rs74315337	0.00024
NM_000261.2(MYOC):c.369C>T (p.Thr123=)	rs75682756	0.00009
NM_000261.2(MYOC):c.244C>T (p.Arg82Cys)	rs764005392	0.00008
NM_000261.2(MYOC):c.864C>T (p.Ile288=)	rs181923440	0.00006
NM_000261.2(MYOC):c.144G>T (p.Gln48His)	rs74315339	0.00001
NM_000261.2(MYOC):c.473G>A (p.Arg158Gln)	rs199746824	0.00001
NM_000261.2(MYOC):c.1020G>A (p.Glu340=)

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