ClinVar Miner

List of variants reported as uncertain significance for Usher syndrome type 2A by Neuberg Centre For Genomic Medicine, NCGM

Included ClinVar conditions (4):

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_206933.4(USH2A):c.2802T>G (p.Cys934Trp)	rs201527662	0.00006
NM_206933.4(USH2A):c.1644+5G>C	rs1558036810
NM_206933.4(USH2A):c.868T>C (p.Ser290Pro)

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