List of variants in gene MYH9 reported as uncertain significance by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 43

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HGVS	dbSNP	gnomAD frequency
NM_002473.6(MYH9):c.*8C>T	rs201455315	0.00081
NM_002473.6(MYH9):c.5026A>G (p.Lys1676Glu)	rs138158369	0.00046
NM_002473.6(MYH9):c.3943-7C>A	rs376396278	0.00032
NM_002473.6(MYH9):c.4831G>A (p.Ala1611Thr)	rs150029980	0.00032
NM_002473.6(MYH9):c.4225G>A (p.Asp1409Asn)	rs34292387	0.00025
NM_002473.6(MYH9):c.4556G>A (p.Ser1519Asn)	rs138193963	0.00016
NM_002473.6(MYH9):c.32A>G (p.Tyr11Cys)	rs201415443	0.00015
NM_002473.6(MYH9):c.928A>G (p.Ile310Val)	rs149789202	0.00013
NM_002473.6(MYH9):c.4247C>T (p.Thr1416Met)	rs758626716	0.00011
NM_002473.6(MYH9):c.5188C>T (p.Arg1730Cys)	rs201021615	0.00009
NM_002473.6(MYH9):c.5338C>T (p.Arg1780Trp)	rs527571090	0.00008
NM_002473.6(MYH9):c.4050G>C (p.Glu1350Asp)	rs375955867	0.00006
NM_002473.6(MYH9):c.4297C>T (p.Arg1433Cys)	rs727503286	0.00005
NM_002473.6(MYH9):c.2159+6C>T	rs748916231	0.00004
NM_002473.6(MYH9):c.193G>A (p.Val65Met)	rs377348805	0.00003
NM_002473.6(MYH9):c.5806C>T (p.Arg1936Trp)	rs727503281	0.00003
NM_002473.6(MYH9):c.1380T>C (p.Asp460=)	rs876657891	0.00002
NM_002473.6(MYH9):c.3082A>G (p.Met1028Val)	rs1205000981	0.00002
NM_002473.6(MYH9):c.491-7G>A	rs200059134	0.00002
NM_002473.6(MYH9):c.833A>G (p.Tyr278Cys)	rs727504863	0.00002
NM_002473.6(MYH9):c.2077C>T (p.Arg693Cys)	rs751852988	0.00001
NM_002473.6(MYH9):c.3397C>G (p.Gln1133Glu)	rs368797590	0.00001
NM_002473.6(MYH9):c.3903G>C (p.Lys1301Asn)	rs767235227	0.00001
NM_002473.6(MYH9):c.4306G>A (p.Ala1436Thr)	rs373912645	0.00001
NM_002473.6(MYH9):c.4448G>A (p.Arg1483Gln)	rs727503285	0.00001
NM_002473.6(MYH9):c.4927C>A (p.Leu1643Met)	rs727504669	0.00001
NM_002473.6(MYH9):c.5177G>A (p.Arg1726His)	rs777701033	0.00001
NM_002473.6(MYH9):c.519-6T>G	rs867195616	0.00001
NM_002473.6(MYH9):c.968T>C (p.Met323Thr)	rs1364094810	0.00001
NM_002473.6(MYH9):c.1468GAG[1] (p.Glu491del)	rs1556635817
NM_002473.6(MYH9):c.170A>T (p.Glu57Val)	rs751041617
NM_002473.6(MYH9):c.19G>T (p.Asp7Tyr)	rs762745890
NM_002473.6(MYH9):c.3215C>T (p.Ala1072Val)	rs1556631812
NM_002473.6(MYH9):c.3272+3G>T	rs1238385506
NM_002473.6(MYH9):c.4179C>G (p.Asp1393Glu)	rs727504829
NM_002473.6(MYH9):c.437T>A (p.Met146Lys)	rs727503294
NM_002473.6(MYH9):c.4598A>G (p.Gln1533Arg)	rs876657892
NM_002473.6(MYH9):c.5107C>T (p.Arg1703Trp)	rs569541375
NM_002473.6(MYH9):c.5225_5239del (p.Gln1742_Glu1746del)	rs876657893
NM_002473.6(MYH9):c.5766-13_5766-2dup	rs1603482655
NM_002473.6(MYH9):c.637C>T (p.Gln213Ter)	rs727503292
NM_002473.6(MYH9):c.659C>T (p.Ala220Val)	rs1190062913
NM_002473.6(MYH9):c.859C>T (p.His287Tyr)	rs727503291

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