ClinVar Miner

Submissions for variant NM_006005.3(WFS1):c.1107_1108insA (p.Ala370fs)

dbSNP: rs2109125327
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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 RCV001667854 SCV001890912 pathogenic Wolfram syndrome 1 criteria provided, single submitter clinical testing

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