List of variants in gene PIGB 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_004855.5(PIGB):c.523-33T>C	rs28459661	0.49472
NM_004855.5(PIGB):c.896G>T (p.Trp299Leu)	rs678892	0.48713
NM_004855.5(PIGB):c.-16A>G	rs28668016	0.22431
NM_004855.5(PIGB):c.485T>C (p.Met162Thr)	rs2290344	0.10822
NM_004855.5(PIGB):c.1504A>G (p.Ser502Gly)	rs652397	0.00464
NM_004855.5(PIGB):c.453T>C (p.Ser151=)	rs35201245	0.00335
NM_004855.5(PIGB):c.971T>C (p.Leu324Ser)	rs73415566	0.00334
NM_004855.5(PIGB):c.1338-11T>C	rs191860992	0.00293
NM_004855.5(PIGB):c.981T>G (p.Phe327Leu)	rs151252589	0.00178
NM_004855.5(PIGB):c.418-4G>A	rs374989533	0.00141
NM_004855.5(PIGB):c.1123+3A>G	rs538622264	0.00108
NM_004855.5(PIGB):c.1337+9del
NM_004855.5(PIGB):c.1338-6dup
NM_004855.5(PIGB):c.1380G>A (p.Pro460=)
NM_004855.5(PIGB):c.202A>T (p.Ile68Leu)
NM_004855.5(PIGB):c.497A>G (p.Glu166Gly)
NM_004855.5(PIGB):c.795-4dup

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