ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.2791+53C>T

gnomAD frequency: 0.94549  dbSNP: rs7577088
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001610466 SCV001832852 benign not provided 2018-06-23 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000156994 SCV000206718 benign Noonan syndrome 2010-12-23 no assertion criteria provided clinical testing

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