ClinVar Miner

List of variants reported as uncertain significance for Noonan syndrome 5

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_002880.3(RAF1):c.1467G>C (p.Leu489Phe) rs1553610155
NM_002880.3(RAF1):c.1814C>T (p.Ser605Phe) rs730881004
NM_002880.3(RAF1):c.601A>G (p.Ile201Val) rs757700986

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