List of variants in gene NRAS reported as likely 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)
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Total variants: 14

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HGVS	dbSNP
NM_002524.4(NRAS):c.-208T>A	rs2273267
NM_002524.5(NRAS):c.2510_2515del	rs549171175
NM_002524.5(NRAS):c.*2662G>A	rs148827219
NM_002524.5(NRAS):c.*2667T>C	rs145382662
NM_002524.5(NRAS):c.*2965del	rs61652108
NM_002524.5(NRAS):c.*3219C>G	rs72994441
NM_002524.5(NRAS):c.*3366G>T	rs72994440
NM_002524.5(NRAS):c.*3384C>T	rs140049110
NM_002524.5(NRAS):c.*346G>A	rs9724642
NM_002524.5(NRAS):c.*3499C>T	rs147926293
NM_002524.5(NRAS):c.*416A>C	rs9724643
NM_002524.5(NRAS):c.*740G>A	rs372008962
NM_002524.5(NRAS):c.*872C>T	rs14804
NM_002524.5(NRAS):c.393C>T (p.His131=)	rs745954671

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