ClinVar Miner

List of variants reported as likely pathogenic 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_206933.4(USH2A):c.11473del (p.His3825fs)	rs774677256	0.00001
NM_206933.4(USH2A):c.14791+5G>T	rs1235430504	0.00001

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