ClinVar Miner

List of variants in gene NRAS reported as benign for Noonan syndrome and Noonan-related syndrome

Included ClinVar conditions (63):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_002524.5(NRAS):c.*872C>T rs14804 0.20324
NM_002524.5(NRAS):c.*687A>G rs9724644 0.02952
NM_002524.5(NRAS):c.*2662G>A rs148827219 0.02701
NM_002524.5(NRAS):c.*2667T>C rs145382662 0.02698
NM_002524.5(NRAS):c.*3384C>T rs140049110 0.00091
NM_002524.5(NRAS):c.*740G>A rs372008962 0.00007
NM_002524.5(NRAS):c.*346G>A rs9724642

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