List of variants reported as uncertain significance for Meier-Gorlin syndrome 3 by Illumina Laboratory Services, Illumina

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_014321.4(ORC6):c.*598G>A	rs201605699	0.00497
NM_014321.4(ORC6):c.*594A>G	rs191163536	0.00350
NM_014321.4(ORC6):c.*640G>A	rs368055096	0.00042
NM_014321.4(ORC6):c.413C>A (p.Pro138Gln)	rs3218745	0.00027
NM_014321.4(ORC6):c.*232A>T	rs531879095	0.00016
NM_014321.4(ORC6):c.*307A>G	rs547544453	0.00014
NM_014321.4(ORC6):c.207T>G (p.Ile69Met)	rs138076975	0.00014
NM_014321.4(ORC6):c.*582A>C	rs570114406	0.00010
NM_014321.4(ORC6):c.196-1G>A	rs748927298	0.00007
NM_014321.4(ORC6):c.556G>T (p.Val186Phe)	rs368692007	0.00007
NM_014321.4(ORC6):c.23G>T (p.Arg8Leu)	rs754832466	0.00003
NM_014321.4(ORC6):c.390A>T (p.Gln130His)	rs372048763	0.00003
NM_014321.4(ORC6):c.450-4G>A	rs886052013	0.00003
NM_014321.4(ORC6):c.96G>C (p.Arg32=)	rs138213159	0.00003
NM_014321.4(ORC6):c.*363C>T	rs768612856	0.00002
NM_014321.4(ORC6):c.-19T>C	rs779856890	0.00002
NM_014321.4(ORC6):c.430G>A (p.Ala144Thr)	rs1369065092	0.00002
NM_014321.4(ORC6):c.*517G>A	rs771044771	0.00001
NM_014321.4(ORC6):c.*621T>C	rs758041096	0.00001
NM_014321.4(ORC6):c.27A>G (p.Leu9=)	rs758376049	0.00001
NM_014321.4(ORC6):c.32C>G (p.Pro11Arg)	rs757562073	0.00001
NM_014321.4(ORC6):c.552G>A (p.Gln184=)	rs74999515	0.00001
NM_014321.4(ORC6):c.592C>T (p.Arg198Trp)	rs376209987	0.00001
NM_014321.4(ORC6):c.*10C>G	rs1405213929
NM_014321.4(ORC6):c.*115T>G	rs886052014
NM_014321.4(ORC6):c.*170C>G	rs577189944
NM_014321.4(ORC6):c.*452C>T	rs768042955
NM_014321.4(ORC6):c.*524A>G	rs1287188674
NM_014321.4(ORC6):c.199del (p.Tyr67fs)	rs1567273817
NM_014321.4(ORC6):c.682C>G (p.Leu228Val)	rs768760107

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