ClinVar Miner

Submissions for variant NM_006005.3(WFS1):c.528_531dup (p.Lys178fs)

dbSNP: rs2109116580
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Endocrinology Laboratory, Christian Medical College RCV001667858 SCV001890918 uncertain significance Wolfram syndrome 1 criteria provided, single submitter clinical testing

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