ClinVar Miner

List of variants reported as uncertain significance for Usher syndrome type 2A by 3billion

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.11366T>C (p.Ile3789Thr)	rs183979371	0.00007
NM_206933.4(USH2A):c.12863C>A (p.Pro4288Gln)	rs1352720909
NM_206933.4(USH2A):c.13339A>G (p.Met4447Val)	rs139474806

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