List of variants in gene FTCD reported as likely pathogenic for hematologic disorder

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_206965.2(FTCD):c.1607T>A (p.Leu536Ter)	rs149266909	0.00116
NM_206965.2(FTCD):c.1068_1098+24del
NM_206965.2(FTCD):c.1261-1G>A
NM_206965.2(FTCD):c.990dup (p.Pro331fs)	rs398124234

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