ClinVar Miner

Submissions for variant NM_014862.4(ARNT2):c.1911A>G (p.Pro637=)

gnomAD frequency: 0.00155  dbSNP: rs149060355
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000904373 SCV001048887 benign not provided 2024-05-09 criteria provided, single submitter clinical testing

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