List of variants in gene CTR9 reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_014633.5(CTR9):c.384+194T>C	rs117966147	0.02396
NM_014633.5(CTR9):c.2728-97C>T	rs117224527	0.01424
NM_014633.5(CTR9):c.1687-3C>T	rs76650154	0.01081
NM_014633.5(CTR9):c.2886-87A>G	rs79355153	0.01005
NM_014633.5(CTR9):c.850-23T>C	rs11822861	0.00890
NM_014633.5(CTR9):c.2373-171G>A	rs115634611	0.00889
NC_000011.10:g.10750932T>C	rs112026705	0.00739
NM_014633.5(CTR9):c.1687-136G>A	rs573689289	0.00739
NM_014633.5(CTR9):c.592+265A>G	rs142214900	0.00688
NM_014633.5(CTR9):c.144+132G>A	rs112818649	0.00686
NM_014633.5(CTR9):c.145-57C>T	rs116871508	0.00651
NM_014633.5(CTR9):c.46-95G>A	rs192886164	0.00645
NM_014633.5(CTR9):c.2886-215T>G	rs77933876	0.00553
NM_014633.5(CTR9):c.742-273C>T	rs142790875	0.00377
NM_014633.5(CTR9):c.2886-139C>T	rs191895962	0.00326
NM_014633.5(CTR9):c.2885+125C>T	rs145313718	0.00278
NM_014633.5(CTR9):c.3449A>G (p.Glu1150Gly)	rs35023148	0.00136
NM_014633.5(CTR9):c.2313T>C (p.Asp771=)	rs138718780	0.00116
NM_014633.5(CTR9):c.1687-137del	rs201006625
NM_014633.5(CTR9):c.1687-139AAAG[2]	rs200086979
NM_014633.5(CTR9):c.2728-109del	rs11386264
NM_014633.5(CTR9):c.3095+232C>A	rs114386774
NM_014633.5(CTR9):c.384+133G>C	rs57192985
NM_014633.5(CTR9):c.502+137C>T	rs145240803
NM_014633.5(CTR9):c.741+170G>A	rs117150241
NM_014633.5(CTR9):c.741+286del	rs147350120
NM_014633.5(CTR9):c.799A>G (p.Ser267Gly)	rs2539377696

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