ClinVar Miner

List of variants reported as uncertain significance for Renpenning syndrome by Illumina Laboratory Services, Illumina

Included ClinVar conditions (1):

Renpenning syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001032382.2(PQBP1):c.*8G>A	rs376272913	0.00003
NM_001032382.2(PQBP1):c.-18-196A>G	rs1006576758	0.00002
NM_001032382.2(PQBP1):c.642-9C>A	rs782015028	0.00001

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