List of variants in gene MYO9A reported as likely 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_006901.4(MYO9A):c.1986+3C>A	rs118109377	0.00497
NM_006901.4(MYO9A):c.6848G>A (p.Arg2283His)	rs142345927	0.00245
NM_006901.4(MYO9A):c.4836C>T (p.Cys1612=)	rs117500002	0.00212
NM_006901.4(MYO9A):c.1845-8T>A	rs201411984	0.00044
NM_006901.4(MYO9A):c.5093A>G (p.Asp1698Gly)	rs150726107	0.00017
NM_006901.4(MYO9A):c.2817C>T (p.Thr939=)	rs375628589	0.00016
NM_006901.4(MYO9A):c.2303G>A (p.Ser768Asn)	rs201780029	0.00013
NM_006901.4(MYO9A):c.1390G>A (p.Glu464Lys)
NM_006901.4(MYO9A):c.1462T>C (p.Leu488=)
NM_006901.4(MYO9A):c.3740A>G (p.Gln1247Arg)
NM_006901.4(MYO9A):c.4332A>G (p.Leu1444=)
NM_006901.4(MYO9A):c.549A>G (p.Leu183=)
NM_006901.4(MYO9A):c.6T>C (p.Asn2=)

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