List of variants in gene MYO7A reported as benign by Eurofins NTD LLC (GA)

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: 22

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HGVS	dbSNP	gnomAD frequency
NM_000260.4(MYO7A):c.4996A>T (p.Ser1666Cys)	rs2276288	0.59864
NM_000260.4(MYO7A):c.5857-7A>T	rs1320703	0.56654
NM_000260.4(MYO7A):c.783T>C (p.Gly261=)	rs762667	0.50077
NM_000260.4(MYO7A):c.4755C>T (p.Ser1585=)	rs7927472	0.47702
NM_000260.4(MYO7A):c.47T>C (p.Leu16Ser)	rs1052030	0.47208
NM_000260.4(MYO7A):c.5156A>G (p.Tyr1719Cys)	rs77625410	0.04825
NM_000260.4(MYO7A):c.468C>T (p.Ile156=)	rs12420129	0.03116
NM_000260.4(MYO7A):c.6424G>A (p.Asp2142Asn)	rs1132036	0.03072
NM_000260.4(MYO7A):c.4589C>T (p.Ser1530Leu)	rs111033183	0.02384
NM_000260.4(MYO7A):c.2035G>A (p.Val679Ile)	rs35641839	0.01879
NM_000260.4(MYO7A):c.5215C>A (p.Arg1739=)	rs111033477	0.00740
NM_000260.4(MYO7A):c.2236G>A (p.Asp746Asn)	rs36090425	0.00646
NM_000260.4(MYO7A):c.4461C>T (p.Asn1487=)	rs56174006	0.00618
NM_000260.4(MYO7A):c.4074C>T (p.Ser1358=)	rs78996818	0.00559
NM_000260.4(MYO7A):c.4697C>T (p.Thr1566Met)	rs41298747	0.00512
NM_000260.4(MYO7A):c.5835C>T (p.Leu1945=)	rs111033476	0.00408
NM_000260.4(MYO7A):c.5866G>A (p.Val1956Ile)	rs142293185	0.00386
NM_000260.4(MYO7A):c.1605C>T (p.Asn535=)	rs111033228	0.00336
NM_000260.4(MYO7A):c.4992C>T (p.Thr1664=)	rs181573957	0.00240
NM_000260.4(MYO7A):c.133-7C>T	rs111033221
NM_000260.4(MYO7A):c.3503+12_3503+33del	rs111033223
NM_000260.4(MYO7A):c.5860C>A (p.Leu1954Ile)	rs948962

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