List of variants in gene PSMB4 reported as benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_002796.3(PSMB4):c.495-40T>C	rs2495391	0.97364
NM_002796.3(PSMB4):c.75G>A (p.Pro25=)	rs7172	0.64309
NM_002796.3(PSMB4):c.701T>C (p.Ile234Thr)	rs4603	0.15159
NM_002796.3(PSMB4):c.347+16A>G	rs16833204	0.00870
NM_002796.3(PSMB4):c.336C>T (p.Leu112=)	rs11557389	0.00196
NM_002796.3(PSMB4):c.577-20T>C	rs200443103	0.00096
NM_002796.3(PSMB4):c.459C>T (p.Asn153=)	rs114882311	0.00065
NM_002796.3(PSMB4):c.18G>A (p.Gly6=)	rs188568243	0.00026
NM_002796.3(PSMB4):c.782+19dup	rs778252922
NM_002796.3(PSMB4):c.783-17_783-16del	rs200105655
NM_002796.3(PSMB4):c.783-18T>C	rs377064071

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