List of variants in gene CPED1 reported as likely 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_024913.5(CPED1):c.416C>T (p.Pro139Leu)	rs137952014	0.00099
NM_024913.5(CPED1):c.2772A>C (p.Ala924=)	rs141494536	0.00084
NM_024913.5(CPED1):c.241A>G (p.Thr81Ala)	rs117047013	0.00071
GRCh37/hg19 7q31.31(chr7:120632159-120893340)x1
NM_024913.5(CPED1):c.1010C>T (p.Ala337Val)	rs148370748
NM_024913.5(CPED1):c.2274T>G (p.Thr758=)	rs1286505445

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