List of variants in gene FKTN reported as likely benign 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001079802.2(FKTN):c.1297A>G (p.Thr433Ala)	rs141918432	0.00228
NM_001079802.2(FKTN):c.167G>A (p.Arg56His)	rs146951171	0.00218
NM_001079802.2(FKTN):c.681G>A (p.Leu227=)	rs142604625	0.00084
NM_001079802.2(FKTN):c.333T>C (p.Thr111=)	rs141729611	0.00015
NM_001079802.2(FKTN):c.444C>T (p.Asp148=)	rs759808323	0.00004
NM_001079802.2(FKTN):c.342A>G (p.Ala114=)	rs368598407	0.00002
NM_001079802.2(FKTN):c.1023G>A (p.Pro341=)	rs146967918
NM_001079802.2(FKTN):c.1185G>A (p.Pro395=)	rs141886790

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