List of variants in gene FKTN reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001079802.2(FKTN):c.166-4A>G	rs193922689	0.00125
NM_001079802.2(FKTN):c.1159G>A (p.Gly387Arg)	rs148975262	0.00051
NM_001079802.2(FKTN):c.1172+13T>C	rs768792475	0.00009
NM_001079802.2(FKTN):c.781-9T>C	rs370564232	0.00006
NM_001079802.2(FKTN):c.869A>T (p.Lys290Ile)	rs755092516	0.00006
NM_001079802.2(FKTN):c.703C>A (p.Pro235Thr)	rs373418195	0.00003
NM_001079802.2(FKTN):c.1298C>T (p.Thr433Met)	rs201590151	0.00001
NM_001079802.2(FKTN):c.105+6T>C	rs754468850
NM_001079802.2(FKTN):c.374G>C (p.Gly125Ala)	rs142783718
NM_001079802.2(FKTN):c.665T>A (p.Val222Asp)
NM_001079802.2(FKTN):c.748T>C (p.Cys250Arg)	rs398123558
NM_001079802.2(FKTN):c.911-13A>G	rs766103012

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