List of variants in gene CPED1 studied for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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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.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.1938T>A (p.Val646=)	rs138199492
NM_024913.5(CPED1):c.2274T>G (p.Thr758=)	rs1286505445

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