List of variants in gene FTCD 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_206965.2(FTCD):c.319T>C (p.Cys107Arg)	rs377359525	0.00033
NM_206965.2(FTCD):c.593G>A (p.Arg198His)	rs142358848	0.00012
NM_206965.2(FTCD):c.236A>C (p.Gln79Pro)	rs775726030	0.00006
NM_206965.2(FTCD):c.1103C>T (p.Ala368Val)	rs1033001525
NM_206965.2(FTCD):c.530G>A (p.Gly177Glu)	rs760709342

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