ClinVar Miner

List of variants reported as likely pathogenic for Noonan syndrome 12

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_012250.6(RRAS2):c.208G>A (p.Ala70Thr)	rs782457908	0.00001
NM_012250.6(RRAS2):c.439C>T (p.Arg147Trp)
NM_012250.6(RRAS2):c.67G>A (p.Gly23Ser)

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