List of variants in gene DRC4 reported as uncertain significance 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_001481.3(DRC4):c.841G>C (p.Asp281His)	rs139167960	0.00058
NM_001481.3(DRC4):c.789C>A (p.Asp263Glu)	rs138733039	0.00050
NM_001481.3(DRC4):c.1306C>T (p.Arg436Cys)	rs555627699	0.00016
NM_001481.3(DRC4):c.558G>C (p.Glu186Asp)	rs200116401	0.00012
NM_001481.3(DRC4):c.1336G>A (p.Gly446Arg)	rs144626445	0.00009
NM_001481.3(DRC4):c.1354G>A (p.Val452Met)	rs147628922	0.00007
NM_001481.3(DRC4):c.1105C>T (p.Arg369Cys)	rs773549442	0.00006
NM_001481.3(DRC4):c.1211G>A (p.Arg404His)	rs755682241	0.00005
NM_001481.3(DRC4):c.125T>C (p.Leu42Pro)	rs2543466092

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