ClinVar Miner

Submissions for variant NM_021975.4(RELA):c.8-10C>T

gnomAD frequency: 0.00104  dbSNP: rs200603499
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001517074 SCV001725485 benign not provided 2024-12-21 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002506620 SCV002811856 likely benign Mucocutaneous ulceration, chronic 2021-07-21 criteria provided, single submitter clinical testing

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