List of variants in gene LRTOMT studied for nonsyndromic genetic hearing loss

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001145308.5(LRTOMT):c.69G>C (p.Leu23=)	rs12272086	0.07159
NM_001145308.4(LRTOMT):c.-602G>A	rs111537544	0.00551
NM_001145308.4(LRTOMT):c.-526T>A	rs190307646	0.00016
NM_001145308.4(LRTOMT):c.-554G>A	rs886048622	0.00005
NM_001145308.4(LRTOMT):c.-422T>C	rs1042068599	0.00004
NM_001145308.4(LRTOMT):c.-453A>G	rs1450426179	0.00004
NM_001145308.4(LRTOMT):c.-379T>C	rs886048625	0.00003
NM_001145308.4(LRTOMT):c.-409G>A	rs886048624
NM_001145308.4(LRTOMT):c.-481G>T	rs886048623

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