List of variants in gene combination LOC130062568, NEDD4L reported as likely benign 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001144967.3(NEDD4L):c.48+11C>G	rs751788981
NM_001144967.3(NEDD4L):c.48+14C>A	rs372316024
NM_001144967.3(NEDD4L):c.48+14C>T	rs372316024

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