ClinVar Miner

Submissions for variant NM_138409.4(MRAP2):c.374G>A (p.Arg125His)

gnomAD frequency: 0.00064  dbSNP: rs115655382
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000882315 SCV001025546 likely benign not provided 2024-12-04 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002487932 SCV002803581 likely benign Body mass index quantitative trait locus 18 2021-07-23 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000882315 SCV005224462 likely benign not provided criteria provided, single submitter not provided

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