ClinVar Miner

Submissions for variant NM_031885.5(BBS2):c.117G>C (p.Lys39Asn)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Developmental Genetics Unit,King Faisal Specialist Hospital & Research Centre	RCV001175187	SCV001338711	likely benign	Bardet-Biedl syndrome 2		no assertion criteria provided	research

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