List of variants in gene SETBP1 reported as not provided

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_015559.3(SETBP1):c.1910C>T (p.Pro637Leu)	rs1011541536	0.00001
NM_015559.3(SETBP1):c.1568del (p.His523fs)	rs886041469
NM_015559.3(SETBP1):c.1765C>T (p.Arg589Ter)	rs1568235086
NM_015559.3(SETBP1):c.1873C>T (p.Arg625Ter)	rs606231272
NM_015559.3(SETBP1):c.2447C>A (p.Thr816Asn)	rs779562371
NM_015559.3(SETBP1):c.2608G>A (p.Gly870Ser)	rs267607040
NM_015559.3(SETBP1):c.2612T>G (p.Ile871Ser)	rs267607038

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