List of variants in gene MYH9 reported as not provided for hematologic disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_002473.6(MYH9):c.136C>T (p.Leu46Phe)	rs147122501	0.00554
NM_002473.6(MYH9):c.2105G>A (p.Arg702His)	rs80338827	0.00001
NM_002473.6(MYH9):c.2290C>T (p.Arg764Cys)	rs1383986403	0.00001
NM_002473.6(MYH9):c.2104C>T (p.Arg702Cys)	rs80338826
NM_002473.6(MYH9):c.2114G>A (p.Arg705His)	rs80338828
NM_002473.6(MYH9):c.279C>G (p.Asn93Lys)	rs121913655
NM_002473.6(MYH9):c.287C>T (p.Ser96Leu)	rs121913657
NM_002473.6(MYH9):c.3493C>T (p.Arg1165Cys)	rs80338829
NM_002473.6(MYH9):c.3494G>T (p.Arg1165Leu)	rs80338830
NM_002473.6(MYH9):c.4270G>A (p.Asp1424Asn)	rs80338831
NM_002473.6(MYH9):c.4270G>C (p.Asp1424His)	rs80338831
NM_002473.6(MYH9):c.4270G>T (p.Asp1424Tyr)	rs80338831
NM_002473.6(MYH9):c.4340A>T (p.Asp1447Val)	rs797044804
NM_002473.6(MYH9):c.5521G>A (p.Glu1841Lys)	rs80338834
NM_002473.6(MYH9):c.5563C>T (p.Arg1855Trp)	rs1436597250
NM_002473.6(MYH9):c.5797C>T (p.Arg1933Ter)	rs80338835
NM_002473.6(MYH9):c.5821del (p.Asp1941fs)	rs587776808

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