ClinVar Miner

Submissions for variant NM_002468.5(MYD88):c.261C>T (p.Gly87=)

gnomAD frequency: 0.00009  dbSNP: rs373382593
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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 RCV000646124 SCV000767881 benign Pyogenic bacterial infections due to MyD88 deficiency 2023-12-15 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003437363 SCV004149378 likely benign not provided 2024-04-01 criteria provided, single submitter clinical testing MYD88: BP4, BP7

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