ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.3964G>A (p.Asp1322Asn)

dbSNP: rs1167931335
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001219741 SCV001391694 uncertain significance RASopathy 2021-08-26 criteria provided, single submitter clinical testing

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