ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.*1694del

dbSNP: rs767903412
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000395195 SCV000430359 uncertain significance Gingival fibromatosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000298776 SCV000430360 uncertain significance Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002502298 SCV002785148 uncertain significance Fibromatosis, gingival, 1; Noonan syndrome 4 2021-07-28 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003418051 SCV004145959 likely benign not provided 2023-05-01 criteria provided, single submitter clinical testing SOS1: BS1

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