ClinVar Miner

Submissions for variant NM_032881.3(LSM10):c.112G>A (p.Val38Met)

gnomAD frequency: 0.00002  dbSNP: rs374549440
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Molecular Biology and Genetics, Istanbul Technical University RCV001251007 SCV001424915 uncertain significance Fraser syndrome 3 no assertion criteria provided research

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