ClinVar Miner

List of variants in gene SPRED1 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_152594.3(SPRED1):c.535G>A (p.Glu179Lys)	rs143121426	0.00001
NM_152594.3(SPRED1):c.578A>G (p.Asn193Ser)	rs766431294	0.00001

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