ClinVar Miner

Submissions for variant NM_052850.4(GADD45GIP1):c.26G>A (p.Arg9His)

gnomAD frequency: 0.00049  dbSNP: rs375539782
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GenomeConnect, ClinGen RCV000845050 SCV000986889 not provided not provided no assertion provided phenotyping only Variant interpretted as Uncertain significance and reported on 10/30/2014 by GTR ID 320384. GenomeConnect assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. GenomeConnect staff make no attempt to reinterpret the clinical significance of the variant.

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