ClinVar Miner

List of variants in gene NRAS reported as likely benign for Noonan syndrome

Included ClinVar conditions (23):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP
NM_002524.4(NRAS):c.*2510_*2515delTAGTTA rs549171175
NM_002524.4(NRAS):c.*2662G>A rs148827219
NM_002524.4(NRAS):c.*2667T>C rs145382662
NM_002524.4(NRAS):c.*2965delT rs61652108
NM_002524.4(NRAS):c.*3219C>G rs72994441
NM_002524.4(NRAS):c.*3366G>T rs72994440
NM_002524.4(NRAS):c.*3384C>T rs140049110
NM_002524.4(NRAS):c.*346G>A rs9724642
NM_002524.4(NRAS):c.*3499C>T rs147926293
NM_002524.4(NRAS):c.*416A>C rs9724643
NM_002524.4(NRAS):c.*740G>A rs372008962
NM_002524.4(NRAS):c.*872C>T rs14804
NM_002524.4(NRAS):c.-208T>A rs2273267

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