List of variants in gene MYO6 studied for Nonsyndromic Hearing Loss, Recessive

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_004999.4(MYO6):c.2535_2538dup	rs149527616	0.00304
NM_004999.4(MYO6):c.*1139del	rs3834289
NM_004999.4(MYO6):c.*1441TAAAT[1]	rs886061769
NM_004999.4(MYO6):c.*2029del	rs886061771
NM_004999.4(MYO6):c.2881_2882del	rs397812617
NM_004999.4(MYO6):c.*2882del	rs397812617
NM_004999.4(MYO6):c.*3301del	rs199966180
NM_004999.4(MYO6):c.*3473del	rs886061777
NM_004999.4(MYO6):c.*4113dup	rs138193115
NM_004999.4(MYO6):c.*4423AATT[1]	rs10547766
NM_004999.4(MYO6):c.*4495AAAT[4]	rs574841371
NM_004999.4(MYO6):c.1078+19dup	rs144408691
NM_004999.4(MYO6):c.1546+7_1546+8del	rs3831003

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