List of variants in gene SPRED1 reported as uncertain significance for Noonan syndrome

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_152594.3(SPRED1):c.836G>A (p.Ser279Asn)	rs904563789	0.00003
NM_152594.3(SPRED1):c.1225_1226delinsTT (p.Ala409Phe)	rs1566877075
NM_152594.3(SPRED1):c.47G>A (p.Arg16Gln)	rs757726772
NM_152594.3(SPRED1):c.854C>T (p.Pro285Leu)	rs759197561

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