List of variants in gene combination LOC126863137, MYH9 reported as likely benign for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_002473.6(MYH9):c.2872G>A (p.Ala958Thr)	rs151036570	0.00066
NM_002473.6(MYH9):c.2808G>A (p.Ala936=)	rs200550959	0.00017
NM_002473.6(MYH9):c.2907C>T (p.Thr969=)	rs767461889	0.00006
NM_002473.6(MYH9):c.2635A>C (p.Met879Leu)	rs200328859	0.00005
NM_002473.6(MYH9):c.2838+19C>T	rs199611979	0.00004
NM_002473.6(MYH9):c.2838+10C>T	rs1027216058	0.00002
NM_002473.6(MYH9):c.2844T>G (p.Leu948=)	rs763022319	0.00002
NM_002473.6(MYH9):c.2632-8_2632-6del	rs773975934
NM_002473.6(MYH9):c.2773GAG[4] (p.Glu929del)
NM_002473.6(MYH9):c.2976+10G>T	rs371839289
NM_002473.6(MYH9):c.2976+9C>T

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