List of variants in gene FKTN reported as benign for not specified

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_001079802.2(FKTN):c.1026C>A (p.Leu342=)	rs17309806	0.27837
NM_001079802.2(FKTN):c.608G>A (p.Arg203Gln)	rs34787999	0.25357
NM_001079802.2(FKTN):c.*2280T>C	rs1024366	0.12115
NM_001079802.2(FKTN):c.373G>A (p.Gly125Ser)	rs34006675	0.03359
NM_001079802.2(FKTN):c.1044+44A>G	rs118064041	0.02504
NM_001079802.2(FKTN):c.166C>T (p.Arg56Cys)	rs41277797	0.02093
NM_001079802.2(FKTN):c.*4825T>C	rs115155934	0.01517
NM_001079802.2(FKTN):c.42G>A (p.Thr14=)	rs78794935	0.01002
NM_001079802.2(FKTN):c.106-40A>G	rs79175958	0.01001
NM_001079802.2(FKTN):c.106-10G>A	rs148384394	0.01000
NM_001079802.2(FKTN):c.-191del	rs138776494	0.00996
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.910+14G>A	rs76180538	0.00806
NM_001079802.2(FKTN):c.-108A>T	rs191502146	0.00604
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.-88-6T>C	rs115730708	0.00212
NM_001079802.2(FKTN):c.-96T>C	rs151250905	0.00201
NM_001079802.2(FKTN):c.681G>A (p.Leu227=)	rs142604625	0.00084
NM_001079802.2(FKTN):c.-77A>G	rs188804693	0.00057
NM_001079802.2(FKTN):c.*4388del	rs148253503
NM_001079802.2(FKTN):c.4397_4401del	rs1047701788
NM_001079802.2(FKTN):c.-45G>T	rs77013649
NM_001079802.2(FKTN):c.-90del	rs727502845

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