List of variants in gene RIT1 reported as benign for Noonan syndrome and Noonan-related 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_006912.6(RIT1):c.-21G>C	rs493446	0.81133
NM_006912.6(RIT1):c.430-7C>T	rs1749409	0.80479
NM_006912.6(RIT1):c.375C>T (p.Asp125=)	rs34831194	0.00759
NM_006912.6(RIT1):c.237+10C>A	rs367785615	0.00014
NM_006912.6(RIT1):c.106+15C>T	rs755316223	0.00006
NM_006912.6(RIT1):c.430-11dup

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