List of variants reported as likely pathogenic for Noonan syndrome 4 by 3billion

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_005633.4(SOS1):c.1132A>G (p.Thr378Ala)	rs397517146
NM_005633.4(SOS1):c.1387C>T (p.Leu463Phe)
NM_005633.4(SOS1):c.1709C>T (p.Pro570Leu)	rs2529034770
NM_005633.4(SOS1):c.805A>G (p.Met269Val)	rs1671005559
NM_005633.4(SOS1):c.925G>A (p.Asp309Asn)	rs397517180

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