ClinVar Miner

Submissions for variant NM_024079.5(ALG8):c.96-291_96-287dup

dbSNP: rs1192507872
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
GeneDx RCV001695620 SCV001914226 benign not provided 2019-10-05 criteria provided, single submitter clinical testing

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