List of variants in gene PIGB reported as likely pathogenic 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004855.5(PIGB):c.695G>A (p.Arg232His)	rs758196959	0.00002
NM_004855.5(PIGB):c.1337+1G>A
NM_004855.5(PIGB):c.522+1G>T
NM_004855.5(PIGB):c.523-2A>G
NM_004855.5(PIGB):c.654-2A>G
NM_004855.5(PIGB):c.795-19T>G
NM_004855.5(PIGB):c.795-1G>C	rs1163732372
NM_004855.5(PIGB):c.795-2A>G

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