Related gene-specific medical variations for Gene (Select 253827) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1324742	NM_001031679.3(MSRB3):c.-147T>G	MSRB3 (M1R)	Single nucleotide variant (5 prime UTR variant +2 more)	Autosomal recessive nonsyndromic hearing loss 74	GLikely pathogenic
Select item 563886	GRCh37/hg19 12q14.3(chr12:65656429-65678117)x1	MSRB3	Copy number loss	not provided	GUncertain significance