List of variants in gene PPP1R15B 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_032833.5(PPP1R15B):c.923G>A (p.Ser308Asn)	rs3014626	0.02685
NM_032833.5(PPP1R15B):c.1886C>G (p.Ser629Cys)	rs111725786	0.00447
NM_032833.5(PPP1R15B):c.430G>A (p.Glu144Lys)	rs4492688	0.00418
NM_032833.5(PPP1R15B):c.156C>T (p.Ser52=)	rs147611819	0.00087
NM_032833.5(PPP1R15B):c.413G>T (p.Ser138Ile)	rs145021449	0.00076
NM_032833.5(PPP1R15B):c.493A>G (p.Ser165Gly)	rs199950235	0.00034
NM_032833.5(PPP1R15B):c.1008A>G (p.Pro336=)
NM_032833.5(PPP1R15B):c.1088A>G (p.Glu363Gly)
NM_032833.5(PPP1R15B):c.1765A>G (p.Lys589Glu)
NM_032833.5(PPP1R15B):c.57G>C (p.Arg19=)
NM_032833.5(PPP1R15B):c.923= (p.Ser308=)

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