ClinVar Miner

Submissions for variant NM_001065.4(TNFRSF1A):c.193+19G>A

gnomAD frequency: 0.00003  dbSNP: rs17847989
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001649033 SCV001863492 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002072994 SCV002334640 benign TNF receptor-associated periodic fever syndrome (TRAPS) 2023-09-19 criteria provided, single submitter clinical testing

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