List of variants in gene KCTD7 reported as 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_153033.5(KCTD7):c.*944C>G	rs9791712	0.67438
NM_153033.5(KCTD7):c.*979C>A	rs9791713	0.67429
NM_153033.5(KCTD7):c.494-149G>C	rs1860470	0.51719
NM_153033.5(KCTD7):c.314+51G>A	rs3764903	0.50189
NM_153033.5(KCTD7):c.493+18_493+21dup	rs57580125	0.11765
NM_153033.5(KCTD7):c.267G>A (p.Thr89=)	rs3764904	0.08655
NM_153033.5(KCTD7):c.144+269C>T	rs12531758	0.03575
NM_153033.5(KCTD7):c.654C>T (p.Asp218=)	rs117194263	0.01460
NM_153033.5(KCTD7):c.315-24C>T	rs75672175	0.01333
NM_153033.5(KCTD7):c.*9G>T	rs116630203	0.00745
NM_153033.5(KCTD7):c.384G>A (p.Glu128=)	rs145238250	0.00147
NM_153033.5(KCTD7):c.273C>T (p.Ser91=)	rs139585796	0.00032
NM_153033.5(KCTD7):c.387C>T (p.Ala129=)	rs140932942	0.00029
NM_153033.5(KCTD7):c.507G>C (p.Arg169=)	rs142379946	0.00028
NM_153033.5(KCTD7):c.687T>C (p.Asp229=)	rs372150992	0.00024
NM_153033.5(KCTD7):c.192A>G (p.Thr64=)	rs142526573	0.00014
NM_153033.5(KCTD7):c.621C>A (p.Leu207=)	rs376944331	0.00010

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