ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.3338-4A>G

gnomAD frequency: 0.00002  dbSNP: rs777684425
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000652812 SCV000774684 uncertain significance Noonan syndrome 9 2023-12-14 criteria provided, single submitter clinical testing This sequence change falls in intron 20 of the SOS2 gene. It does not directly change the encoded amino acid sequence of the SOS2 protein. This variant is present in population databases (rs777684425, gnomAD 0.007%). This variant has been observed in individual(s) with SOS2-related conditions (Invitae). ClinVar contains an entry for this variant (Variation ID: 542397). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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