ClinVar Miner

List of variants in gene combination HRAS, LRRC56 reported as likely pathogenic for Noonan syndrome 3

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Total variants: 2
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HGVS dbSNP
NM_005343.4(HRAS):c.181C>A (p.Gln61Lys) rs28933406
NM_005343.4(HRAS):c.183G>T (p.Gln61His) rs121913496

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