List of variants in gene NEDD4L reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_001144967.3(NEDD4L):c.965A>G (p.Asn322Ser)	rs749019037	0.00005
NM_001144967.3(NEDD4L):c.1691C>A (p.Thr564Lys)	rs769198983	0.00004
NM_001144967.3(NEDD4L):c.2273A>G (p.Asn758Ser)	rs202127939	0.00004
NM_001144967.3(NEDD4L):c.871C>G (p.Leu291Val)	rs773477776	0.00004
NM_001144967.3(NEDD4L):c.1877A>C (p.Asn626Thr)	rs1008436842	0.00003
NM_001144967.3(NEDD4L):c.2093A>G (p.Asn698Ser)	rs377143286	0.00003
NM_001144967.3(NEDD4L):c.1316C>T (p.Pro439Leu)	rs775630982	0.00002
NM_001144967.3(NEDD4L):c.1457A>G (p.Asn486Ser)	rs965302278	0.00002
NM_001144967.3(NEDD4L):c.1882T>A (p.Phe628Ile)	rs1477791039	0.00002
NM_001144967.3(NEDD4L):c.2665C>T (p.Leu889Phe)	rs775922627	0.00002
NM_001144967.3(NEDD4L):c.2873G>A (p.Arg958Gln)	rs777624478	0.00002
NM_001144967.3(NEDD4L):c.740G>A (p.Arg247Gln)	rs747072217	0.00002
NM_001144967.3(NEDD4L):c.1033G>A (p.Asp345Asn)	rs375898604	0.00001
NM_001144967.3(NEDD4L):c.1535G>A (p.Arg512Gln)	rs1365042367	0.00001
NM_001144967.3(NEDD4L):c.1676A>G (p.His559Arg)	rs958611451	0.00001
NM_001144967.3(NEDD4L):c.2205T>G (p.Phe735Leu)	rs1242218314	0.00001
NM_001144967.3(NEDD4L):c.2465A>C (p.Lys822Thr)	rs778557607	0.00001
NM_001144967.3(NEDD4L):c.534C>G (p.Asp178Glu)	rs903587997	0.00001
NM_001144967.3(NEDD4L):c.1132G>A (p.Val378Met)	rs2145157218
NM_001144967.3(NEDD4L):c.1483A>G (p.Thr495Ala)	rs1297218616
NM_001144967.3(NEDD4L):c.1523C>T (p.Ala508Val)	rs573738976
NM_001144967.3(NEDD4L):c.1607T>G (p.Met536Arg)	rs369952868
NM_001144967.3(NEDD4L):c.812A>C (p.Glu271Ala)	rs1404724194

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