List of variants in gene USH2A reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_206933.4(USH2A):c.6713A>C (p.Glu2238Ala)	rs41277212	0.01991
NM_206933.4(USH2A):c.2109T>C (p.Asp703=)	rs45555435	0.01476
NM_206933.4(USH2A):c.15091C>T (p.Arg5031Trp)	rs56038610	0.01377
NM_206933.4(USH2A):c.11677C>A (p.Pro3893Thr)	rs41303285	0.01316
NM_206933.4(USH2A):c.1434G>C (p.Glu478Asp)	rs35730265	0.01315
NM_206933.4(USH2A):c.688G>A (p.Val230Met)	rs45500891	0.01191
NM_206933.4(USH2A):c.11928G>A (p.Thr3976=)	rs55961436	0.01005
NM_206933.4(USH2A):c.12445T>C (p.Trp4149Arg)	rs115884084	0.00956
NM_206933.4(USH2A):c.848+5G>C	rs74329863	0.00641
NM_206933.4(USH2A):c.12608A>G (p.Gln4203Arg)	rs148556640	0.00247
NM_206933.4(USH2A):c.3364T>G (p.Ser1122Ala)	rs148135241	0.00152
NM_206933.4(USH2A):c.7068T>G (p.Asn2356Lys)	rs200038092	0.00051
NM_206933.4(USH2A):c.10062G>C (p.Val3354=)	rs200172376	0.00020
NM_206933.4(USH2A):c.10510C>G (p.Pro3504Ala)	rs200372118	0.00020
NM_206933.4(USH2A):c.14662A>T (p.Thr4888Ser)	rs200993435	0.00004
NM_206933.4(USH2A):c.7334C>T (p.Ser2445Phe)	rs41315579	0.00001
NM_206933.4(USH2A):c.2993+715_2993+716insATATATATATATTATATATATAAT

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