ClinVar Miner

Submissions for variant NM_002184.4(IL6ST):c.1301C>G (p.Pro434Arg)

gnomAD frequency: 0.00100  dbSNP: rs140433866
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 RCV001522027 SCV001731488 benign not provided 2024-12-31 criteria provided, single submitter clinical testing

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