ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.2964+32T>G

dbSNP: rs727505384
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000156986 SCV000206708 benign Noonan syndrome 2012-05-31 no assertion criteria provided clinical testing

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