List of variants in gene SPRED1 reported as likely benign 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.535G>A (p.Glu179Lys)	rs143121426	0.00001
NM_152594.3(SPRED1):c.997T>G (p.Ser333Ala)	rs1222580149	0.00001
NM_152594.3(SPRED1):c.1285T>C (p.Cys429Arg)	rs2542744607
NM_152594.3(SPRED1):c.282T>G (p.Ile94Met)	rs1160225934

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