List of variants in gene PQBP1 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001032382.2(PQBP1):c.67+205C>A	rs369754874	0.01267
NM_001032382.2(PQBP1):c.577+25G>A	rs142702270	0.00512
NM_001032382.2(PQBP1):c.356G>A (p.Arg119His)	rs781981660	0.00007
NM_001032382.2(PQBP1):c.397C>T (p.Arg133Trp)	rs201489630	0.00005
NM_001032382.2(PQBP1):c.384C>T (p.His128=)	rs782819795	0.00004
NM_001032382.2(PQBP1):c.690C>T (p.Gly230=)	rs367752180	0.00004
NM_001032382.2(PQBP1):c.292+6T>G	rs781958954	0.00003
NM_001032382.2(PQBP1):c.492G>T (p.Gly164=)	rs375706327	0.00003
NM_001032382.2(PQBP1):c.391T>C (p.Ser131Pro)	rs782016622	0.00001
NM_001032382.2(PQBP1):c.510G>A (p.Arg170=)	rs782103312	0.00001

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