ClinVar Miner

List of variants reported as uncertain significance for Noonan syndrome 5 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002880.4(RAF1):c.1879C>T (p.Arg627Trp)	rs730881005	0.00003
NM_002880.4(RAF1):c.1296C>A (p.His432Gln)
NM_002880.4(RAF1):c.1850A>C (p.Asn617Thr)	rs933142627

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