List of variants in gene combination CERS1, GDF1 reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001492.6(GDF1):c.326-14T>C	rs4808864	0.99989
NM_021267.5(CERS1):c.*151G>T	rs11667388	0.99905
NM_001492.6(GDF1):c.353C>T (p.Ala118Val)	rs4808863	0.30267
NM_001492.6(GDF1):c.-1089T>C	rs113536478	0.25589
NM_001492.6(GDF1):c.-422-11C>T	rs2075762	0.09802
NM_001492.6(GDF1):c.325+20G>A	rs146219830	0.00363
NM_001492.6(GDF1):c.-894A>G	rs200107216	0.00064
NM_001492.6(GDF1):c.456GGC[6] (p.Ala158_Pro159insAla)	rs571387097
NM_001492.6(GDF1):c.469_470insGCG (p.Ala156_Ala157insGly)	rs2145986398

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