List of variants in gene MYO15A reported as benign by Illumina Laboratory Services, Illumina

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.7185T>C (p.Phe2395=)	rs2955379	0.99481
NM_016239.4(MYO15A):c.5929T>C (p.Cys1977Arg)	rs854777	0.79149
NM_016239.4(MYO15A):c.10431T>C (p.Tyr3477=)	rs854800	0.78890
NM_016239.4(MYO15A):c.*920G>A	rs854802	0.78850
NM_016239.4(MYO15A):c.5826-12A>C	rs854778	0.76256
NM_016239.4(MYO15A):c.7857G>A (p.Gly2619=)	rs854772	0.55976
NM_016239.4(MYO15A):c.4954C>T (p.Leu1652=)	rs2280777	0.52028
NM_016239.4(MYO15A):c.-219-14T>C	rs854817	0.45512
NM_016239.4(MYO15A):c.-76A>C	rs854818	0.45498
NM_016239.4(MYO15A):c.1899A>G (p.Pro633=)	rs2955366	0.41355
NM_016239.4(MYO15A):c.1783G>A (p.Ala595Thr)	rs2955365	0.39950
NM_016239.4(MYO15A):c.8322C>T (p.Ser2774=)	rs712272	0.34416
NM_016239.4(MYO15A):c.8045A>T (p.Tyr2682Phe)	rs712270	0.34278
NM_016239.4(MYO15A):c.8460-15C>T	rs861278	0.34259
NM_016239.4(MYO15A):c.2152T>G (p.Trp718Gly)	rs2955367	0.34123
NM_016239.4(MYO15A):c.9518-11T>C	rs62073604	0.19159
NM_016239.4(MYO15A):c.9486C>T (p.Asp3162=)	rs8077577	0.19129
NM_016239.4(MYO15A):c.*612C>G	rs10048161	0.17931
NM_016239.4(MYO15A):c.5212-14C>T	rs2072652	0.16745
NM_016239.4(MYO15A):c.6052G>A (p.Gly2018Arg)	rs2272571	0.16711
NM_016239.4(MYO15A):c.5649+14G>A	rs2072653	0.15358
NM_016239.4(MYO15A):c.7468G>A (p.Ala2490Thr)	rs16960959	0.03924
NM_016239.4(MYO15A):c.8339C>T (p.Thr2780Met)	rs143826293	0.00394
NM_016239.4(MYO15A):c.8088+5C>G	rs9916193

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