ClinVar Miner

Submissions for variant NM_000053.4(ATP7B):c.3526G>T (p.Gly1176Ter) (rs137853279)

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
ClinVar Staff, National Center for Biotechnology Information (NCBI)	RCV000144371	SCV000189438	not provided	Wilson disease		no assertion provided	not provided

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