ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.315+327G>A

dbSNP: rs2133587175
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
Invitae RCV001484376 SCV001688794 likely benign not provided 2022-01-17 criteria provided, single submitter clinical testing

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