List of variants in gene NDUFB9 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: 20

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HGVS	dbSNP	gnomAD frequency
NM_005005.3(NDUFB9):c.101+240G>C	rs7011005	0.01131
NM_005005.3(NDUFB9):c.102-75A>T	rs9297694	0.00877
NM_005005.3(NDUFB9):c.295-192C>G	rs115449696	0.00590
NC_000008.11:g.124550169G>A	rs76433478	0.00484
NC_000008.11:g.124550012T>C	rs115878135	0.00373
NM_005005.3(NDUFB9):c.-18G>T	rs199613912	0.00118
NM_005005.3(NDUFB9):c.294+13T>C	rs146951703	0.00031
NM_005005.3(NDUFB9):c.23C>T (p.Pro8Leu)	rs755557988	0.00025
NM_005005.3(NDUFB9):c.-31C>T	rs534646199	0.00004
NM_005005.3(NDUFB9):c.477G>A (p.Lys159=)	rs774020236	0.00003
NM_005005.3(NDUFB9):c.174G>A (p.Ala58=)	rs1344199544	0.00002
NM_005005.3(NDUFB9):c.-26C>T	rs754423576	0.00001
NM_005005.3(NDUFB9):c.530G>A (p.Arg177Gln)	rs780144498	0.00001
NM_005005.3(NDUFB9):c.-47G>T	rs866600933
NM_005005.3(NDUFB9):c.-51A>G	rs371001929
NM_005005.3(NDUFB9):c.102-280_102-273del	rs1176273075
NM_005005.3(NDUFB9):c.294+223G>A	rs113696540
NM_005005.3(NDUFB9):c.364A>C (p.Arg122=)	rs1167377589
NM_005005.3(NDUFB9):c.408+295_408+299del	rs374799342
NM_005005.3(NDUFB9):c.409-239T>A	rs56280096

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