ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.15179A>G (p.His5060Arg)

dbSNP: rs886038444
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
PreventionGenetics, part of Exact Sciences RCV000253344 SCV000307236 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001722303 SCV000519866 likely benign not provided 2021-03-30 criteria provided, single submitter clinical testing

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