Variants in gene MYO15A with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 14

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.8090T>C (p.Val2697Ala)	rs200451098	0.00013
NM_016239.4(MYO15A):c.9861C>T (p.Gly3287=)	rs372466080	0.00011
NM_016239.4(MYO15A):c.4777G>A (p.Glu1593Lys)	rs376469502	0.00008
NM_016239.4(MYO15A):c.8050T>C (p.Tyr2684His)	rs376351191	0.00007
NM_016239.4(MYO15A):c.5925G>A (p.Trp1975Ter)	rs375290498	0.00005
NM_016239.4(MYO15A):c.4642G>A (p.Ala1548Thr)	rs201067821	0.00002
NM_016239.4(MYO15A):c.7788-10A>G	rs369105885	0.00002
NM_016239.4(MYO15A):c.10263C>G (p.Ile3421Met)	rs748246442	0.00001
NM_016239.4(MYO15A):c.6634G>A (p.Glu2212Lys)	rs371352836	0.00001
NM_016239.4(MYO15A):c.6787G>A (p.Gly2263Ser)	rs375459945	0.00001
NM_016239.4(MYO15A):c.10247CCT[1] (p.Ser3417del)	rs760069953
NM_016239.4(MYO15A):c.5809C>T (p.Arg1937Cys)	rs749465098
NM_016239.4(MYO15A):c.6589C>T (p.Gln2197Ter)	rs779445819
NM_016239.4(MYO15A):c.92del (p.Lys31fs)

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