"Fulgent Genetics, Fulgent Genetics"[submitter] AND "LOC126863137"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1223302	NM_002473.6(MYH9):c.2913G>A (p.Ala971=)	LOC126863137, MYH9	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 1593559	NM_002473.6(MYH9):c.2844T>G (p.Leu948=)	LOC126863137, MYH9	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 17 +2 more	GLikely benign
Select item 1204293	NM_002473.6(MYH9):c.2838+19C>T	LOC126863137, MYH9	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 1553602	NM_002473.6(MYH9):c.2838+10C>T	LOC126863137, MYH9	Single nucleotide variant (intron variant)	not provided +2 more	GLikely benign
Select item 258736	NM_002473.6(MYH9):c.2808G>A (p.Ala936=)	LOC126863137, MYH9	Single nucleotide variant (synonymous variant)	Kidney disorder +4 more	GBenign/Likely benign
Select item 164448	NM_002473.6(MYH9):c.2714G>A (p.Arg905His)	LOC126863137, MYH9 (R905H)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 17 +3 more	GConflicting classifications of pathogenicity
Select item 1696936	NM_002473.6(MYH9):c.2713C>T (p.Arg905Cys)	LOC126863137, MYH9 (R905C)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 17 +2 more	GConflicting classifications of pathogenicity

ClinVar