List of variants in gene CPED1 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_024913.5(CPED1):c.2846A>C (p.Lys949Thr)	rs798911	0.01859
NM_024913.5(CPED1):c.2634-3C>A	rs60982266	0.00804
NM_024913.5(CPED1):c.879A>G (p.Thr293=)	rs113695658	0.00710
NM_024913.5(CPED1):c.420G>A (p.Gly140=)	rs34283669	0.00549
NM_024913.5(CPED1):c.1938T>A (p.Val646=)	rs138199492

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