List of variants in gene FKTN reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001079802.2(FKTN):c.1336A>G (p.Asn446Asp)	rs41313301	0.00809
NM_001079802.2(FKTN):c.166-6A>G	rs41277795	0.00808
NM_001079802.2(FKTN):c.1045-40C>A	rs145883833	0.00284
NM_001079802.2(FKTN):c.668C>T (p.Thr223Ile)	rs116105846	0.00224
NM_001079802.2(FKTN):c.-96T>C	rs151250905	0.00201
NM_001079802.2(FKTN):c.166-4A>G	rs193922689	0.00125
NM_001079802.2(FKTN):c.681G>A (p.Leu227=)	rs142604625	0.00084
NM_001079802.2(FKTN):c.910+13C>T	rs375259473	0.00026
NM_001079802.2(FKTN):c.1172+13T>C	rs768792475	0.00009
NM_001079802.2(FKTN):c.869A>T (p.Lys290Ile)	rs755092516	0.00006
NM_001079802.2(FKTN):c.370-50T>C	rs139910824	0.00005
NM_001079802.2(FKTN):c.1228C>A (p.His410Asn)	rs146272618	0.00004
NM_001079802.2(FKTN):c.911-8C>A	rs749557617	0.00003
NM_001079802.2(FKTN):c.357A>G (p.Leu119=)	rs760933616	0.00001
NM_001079802.2(FKTN):c.166-9C>T	rs1361772036
NM_001079802.2(FKTN):c.647+30A>T
NM_001079802.2(FKTN):c.766C>A (p.Arg256=)	rs377417974

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