List of variants in gene PQBP1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001032382.2(PQBP1):c.264G>A (p.Ser88=)	rs398124212	0.00018
NM_001032382.2(PQBP1):c.585C>T (p.Ser195=)	rs149688357	0.00011
NM_001032382.2(PQBP1):c.356G>A (p.Arg119His)	rs781981660	0.00007
NM_001032382.2(PQBP1):c.510G>A (p.Arg170=)	rs782103312	0.00001
NM_001032382.2(PQBP1):c.277A>C (p.Arg93=)
NM_001032382.2(PQBP1):c.334_354del (p.Gly113_Arg119del)	rs606231198
NM_001032382.2(PQBP1):c.99T>C (p.Tyr33=)

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