List of variants in gene USH2A reported as uncertain significance by Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

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

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_206933.4(USH2A):c.9882C>G (p.Cys3294Trp)	rs749228276	0.00003
NM_206933.4(USH2A):c.9921T>G (p.Cys3307Trp)	rs1057519382	0.00002
NM_206933.4(USH2A):c.15188T>C (p.Leu5063Pro)	rs376816523	0.00001
NM_206933.4(USH2A):c.7412T>A (p.Leu2471His)	rs1290644032	0.00001
NM_206933.4(USH2A):c.9433C>T (p.Leu3145Phe)	rs267598373	0.00001
NM_206933.4(USH2A):c.10485AGA[1] (p.Glu3496del)	rs1241034250
NM_206933.4(USH2A):c.13339A>G (p.Met4447Val)	rs139474806
NM_206933.4(USH2A):c.1606T>A (p.Cys536Ser)	rs111033273
NM_206933.4(USH2A):c.1813T>C (p.Cys605Arg)	rs886043096
NM_206933.4(USH2A):c.4027A>C (p.Asn1343His)	rs754634823
NM_206933.4(USH2A):c.6163G>A (p.Ala2055Thr)	rs768233523
NM_206933.4(USH2A):c.7915T>C (p.Ser2639Pro)	rs398124620
NM_206933.4(USH2A):c.8395G>T (p.Gly2799Cys)	rs1026326311
NM_206933.4(USH2A):c.9335_9358del (p.Asp3112_Arg3119del)	rs773379163

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