List of variants in gene IQCB1 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001023570.4(IQCB1):c.1441G>A (p.Glu481Lys)	rs140630401	0.00145
NM_001023570.4(IQCB1):c.1703T>C (p.Leu568Pro)	rs145400780	0.00143
NM_001023570.4(IQCB1):c.782T>G (p.Leu261Arg)	rs199959360	0.00040
NM_001023570.4(IQCB1):c.348A>G (p.Leu116=)	rs139299149	0.00004
NM_001023570.4(IQCB1):c.1191T>C (p.His397=)	rs556134592	0.00003
NM_001023570.4(IQCB1):c.101-9T>A	rs753647177	0.00001
NM_001023570.4(IQCB1):c.1568-10T>C	rs762667783	0.00001
NM_001023570.4(IQCB1):c.776G>A (p.Arg259His)	rs374034270	0.00001
NM_001023570.4(IQCB1):c.1410+18C>T	rs886038375
NM_001023570.4(IQCB1):c.1416T>G (p.Ser472=)

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