ClinVar Miner

Submissions for variant NM_005676.5(RBM10):c.1104A>G (p.Pro368=)

gnomAD frequency: 0.00081  dbSNP: rs149109733
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
Eurofins Ntd Llc (ga) RCV000322295 SCV000344625 uncertain significance not provided 2016-08-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000322295 SCV001084404 benign not provided 2023-12-25 criteria provided, single submitter clinical testing

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