ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.3460-2A>C

dbSNP: rs281865159
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000032138 SCV000055697 not provided Werner syndrome no assertion provided literature only Potential founder variant in the Turkish population. Results in exon 30 deletion.

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