List of variants in gene FKTN reported as benign by Illumina Laboratory Services, Illumina

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001079802.2(FKTN):c.*5618T>A	rs1048215	0.12282
NM_001079802.2(FKTN):c.*786T>G	rs10978177	0.12279
NM_001079802.2(FKTN):c.*1133A>G	rs2768282	0.12157
NM_001079802.2(FKTN):c.*2280T>C	rs1024366	0.12115
NM_001079802.2(FKTN):c.*5260G>T	rs2010861	0.11975
NM_001079802.2(FKTN):c.*5041G>A	rs1854124	0.11478
NM_001079802.2(FKTN):c.*5062G>A	rs1854125	0.07482
NM_001079802.2(FKTN):c.*3778T>C	rs79831528	0.02904
NM_001079802.2(FKTN):c.166C>T (p.Arg56Cys)	rs41277797	0.02093
NM_001079802.2(FKTN):c.*2298C>G	rs116107812	0.01491
NM_001079802.2(FKTN):c.*5517T>C	rs114655654	0.01215
NM_001079802.2(FKTN):c.*1638A>G	rs78462952	0.00980
NM_001079802.2(FKTN):c.*1843A>T	rs117283748	0.00026
NM_001079802.2(FKTN):c.*806G>C	rs75971372
NM_001079802.2(FKTN):c.-45G>T	rs77013649

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