ClinVar Miner

Submissions for variant NM_030665.4(RAI1):c.5023G>C (p.Val1675Leu)

gnomAD frequency: 0.00003  dbSNP: rs113210810
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000177364 SCV000229213 uncertain significance not provided 2014-06-22 criteria provided, single submitter clinical testing
GeneDx RCV000177364 SCV001845937 benign not provided 2019-12-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000177364 SCV002463949 benign not provided 2024-01-29 criteria provided, single submitter clinical testing

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