ClinVar Miner

Submissions for variant NM_012452.3(TNFRSF13B):c.618C>T (p.Ala206=) (rs147846226)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000895395 SCV001039432 benign Common variable immunodeficiency 2 2019-12-31 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV001201259 SCV001372364 benign not specified 2020-06-11 criteria provided, single submitter clinical testing

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