List of variants in gene CTSF 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_003793.4(CTSF):c.676C>T (p.Arg226Cys)	rs143313688	0.00259
NM_003793.4(CTSF):c.683C>G (p.Thr228Arg)	rs148611356	0.00107
NM_003793.4(CTSF):c.214-6C>T	rs376579629	0.00026
NM_003793.4(CTSF):c.531+3G>C	rs150926626	0.00001
NM_003793.4(CTSF):c.1450G>C (p.Asp484His)	rs2134948341
NM_003793.4(CTSF):c.200_205dup (p.Gly67_Arg68dup)	rs772656687

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