ClinVar Miner

Submissions for variant NM_005357.4(LIPE):c.436C>T (p.Pro146Ser)

gnomAD frequency: 0.00857  dbSNP: rs34348028
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000889135 SCV001032797 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV003151185 SCV003839676 benign not specified 2022-08-08 no assertion criteria provided clinical testing

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