List of variants in gene FAM161A 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001201543.2(FAM161A):c.1133T>G (p.Leu378Arg)	rs187695569	0.00389
NM_001201543.2(FAM161A):c.1759G>A (p.Glu587Lys)	rs868226745	0.00004
NM_001201543.2(FAM161A):c.1004G>A (p.Arg335Gln)	rs755314585	0.00002
NM_001201543.2(FAM161A):c.1804G>A (p.Glu602Lys)	rs769359884	0.00001
NM_001201543.2(FAM161A):c.1484G>A (p.Arg495His)	rs201998260

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