List of variants in gene SPRED1 reported as uncertain significance by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_152594.3(SPRED1):c.1273A>G (p.Met425Val)	rs368307475	0.00006
NM_152594.3(SPRED1):c.424G>T (p.Ala142Ser)	rs763971890	0.00001
NM_152594.3(SPRED1):c.517A>G (p.Ile173Val)	rs1060502504	0.00001
NM_152594.3(SPRED1):c.50T>C (p.Val17Ala)	rs1421913267
NM_152594.3(SPRED1):c.546T>A (p.Asn182Lys)	rs1419303814

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