List of variants in gene FKBP14 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_017946.4(FKBP14):c.568_570del (p.Lys190del)	rs762279651	0.00039
NM_017946.4(FKBP14):c.357T>G (p.Ile119Met)	rs202182643	0.00010
NM_017946.4(FKBP14):c.144G>A (p.Met48Ile)	rs141850025	0.00009
NM_017946.4(FKBP14):c.224T>G (p.Ile75Ser)	rs763688956	0.00001
NM_017946.4(FKBP14):c.161G>C (p.Gly54Ala)
NM_017946.4(FKBP14):c.376A>G (p.Ile126Val)	rs1789964659

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