List of variants in gene CTSF reported as benign for hereditary dementia

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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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.126C>T (p.Pro42=)	rs1044522	0.22868
NM_003793.4(CTSF):c.722-5C>T	rs78871927	0.06870
NM_003793.4(CTSF):c.418G>A (p.Ala140Thr)	rs79274952	0.01384
NM_003793.4(CTSF):c.1322-19G>A	rs73505406	0.00770
NM_003793.4(CTSF):c.1368C>T (p.Asp456=)	rs148155987	0.00759
NM_003793.4(CTSF):c.939G>A (p.Gly313=)	rs114727660	0.00758
NM_003793.4(CTSF):c.1261C>T (p.Arg421Trp)	rs28464796	0.00735
NM_003793.4(CTSF):c.1158C>T (p.Asn386=)	rs116329758	0.00447
NM_003793.4(CTSF):c.458A>G (p.Gln153Arg)	rs11550508	0.00311
NM_003793.4(CTSF):c.1231-13T>C	rs199830949	0.00298
NM_003793.4(CTSF):c.130C>T (p.Arg44Cys)	rs573483617	0.00221
NM_003793.4(CTSF):c.1321C>T (p.Arg441Cys)	rs150922871	0.00177
NM_003793.4(CTSF):c.1407C>T (p.Ser469=)	rs144556402	0.00039
NM_003793.4(CTSF):c.45G>T (p.Pro15=)	rs117792851	0.00020

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