ClinVar Miner

Submissions for variant NM_020975.6(RET):c.898G>A (p.Asp300Asn)

dbSNP: rs2132719351
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Lab, University of California San Francisco RCV001376021 SCV001573031 uncertain significance Hirschsprung disease, susceptibility to, 1 2020-08-06 criteria provided, single submitter clinical testing

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