List of variants in gene MSRB3 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001031679.3(MSRB3):c.77-2A>G	rs145704693	0.00004
NM_001031679.3(MSRB3):c.55C>T (p.Arg19Ter)	rs149258390	0.00002
NM_001031679.3(MSRB3):c.244T>G (p.Cys82Gly)	rs387907088	0.00001
NM_001031679.3(MSRB3):c.391-1G>A	rs751906778	0.00001
NM_001031679.3(MSRB3):c.-147T>G	rs949229098
NM_001031679.3(MSRB3):c.-51-1502G>A	rs2136420609
NM_001031679.3(MSRB3):c.238GTT[1] (p.Val81del)
NM_001031679.3(MSRB3):c.293-2A>G
NM_001031679.3(MSRB3):c.383G>A (p.Cys128Tyr)
NM_001031679.3(MSRB3):c.406G>A (p.Gly136Arg)	rs2136722469

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