ClinVar Miner

Submissions for variant NM_198407.2(GHSR):c.*1676_*1679del (rs150657222)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000339492 SCV000442131 likely benign Short stature, idiopathic, autosomal 2016-06-14 criteria provided, single submitter clinical testing

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