List of variants in gene FTCD reported as uncertain significance by Eurofins NTD LLC (GA)

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_206965.2(FTCD):c.430G>A (p.Gly144Arg)	rs138139105	0.00022
NM_206965.2(FTCD):c.1448C>T (p.Ala483Val)	rs145609043	0.00016
NM_206965.2(FTCD):c.677T>C (p.Leu226Pro)	rs149445900	0.00012
NM_206965.2(FTCD):c.236A>C (p.Gln79Pro)	rs775726030	0.00006
NM_206965.2(FTCD):c.1480G>A (p.Ala494Thr)	rs398124233	0.00003
NM_206965.2(FTCD):c.197C>T (p.Ala66Val)	rs199867833	0.00002
NM_206965.2(FTCD):c.274C>T (p.Pro92Ser)	rs749149640	0.00001
NM_206965.2(FTCD):c.424C>T (p.Arg142Trp)	rs746980247	0.00001
NM_206965.2(FTCD):c.1583A>C (p.Gln528Pro)	rs727503938

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