List of variants in gene CTSF reported as benign 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_003793.4(CTSF):c.1401T>C (p.Arg467=)	rs572846	0.62182
NM_003793.4(CTSF):c.762G>A (p.Arg254=)	rs545009	0.62158
NM_003793.4(CTSF):c.219T>C (p.Gly73=)	rs1127894	0.62142
NM_003793.4(CTSF):c.722-5C>T	rs78871927	0.06870
NM_003793.4(CTSF):c.1368C>T (p.Asp456=)	rs148155987	0.00759
NM_003793.4(CTSF):c.531+27_531+42del	rs527638704

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