List of variants in gene MYO15A reported as uncertain significance for Hearing impairment

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.7984C>G (p.Leu2662Val)	rs200930743	0.00058
NM_016239.4(MYO15A):c.10181C>T (p.Ala3394Val)	rs200249886	0.00024
NM_016239.4(MYO15A):c.8281G>A (p.Val2761Met)	rs367717396	0.00004
NM_016239.4(MYO15A):c.9515A>G (p.Gln3172Arg)	rs375465287	0.00002
NM_016239.4(MYO15A):c.3646C>T (p.Arg1216Cys)	rs547573001	0.00001
NM_016239.4(MYO15A):c.5491G>A (p.Gly1831Arg)	rs1260018632	0.00001
NM_016239.4(MYO15A):c.1238G>C (p.Trp413Ser)	rs2142245203
NM_016239.4(MYO15A):c.266A>C (p.Gln89Pro)	rs2142237084
NM_016239.4(MYO15A):c.8261C>T (p.Thr2754Met)	rs766544188
NM_016239.4(MYO15A):c.9583C>T (p.Pro3195Ser)	rs2142402540

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