ClinVar Miner

Submissions for variant NM_001083602.2(PTCH1):c.2689+21A>G (rs2236406)

Minimum review status:		Collection method:
Minimum conflict level:
		ClinVar version:

Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
PreventionGenetics,PreventionGenetics	RCV000244081	SCV000303341	benign	not specified		criteria provided, single submitter	clinical testing

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