List of variants in gene MYH11 reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_002474.3(MYH11):c.1749+4C>G	rs776271431	0.00015
NM_002474.3(MYH11):c.3530C>T (p.Thr1177Met)	rs201391947	0.00011
NM_002474.3(MYH11):c.3293+5C>T	rs766421052	0.00008
NM_002474.3(MYH11):c.1301G>A (p.Arg434His)	rs754636432	0.00006
NM_002474.3(MYH11):c.3858+13C>T	rs375738696	0.00006
NM_002474.3(MYH11):c.1768G>A (p.Ala590Thr)	rs745516001	0.00004
NM_002474.3(MYH11):c.2579A>T (p.Glu860Val)	rs373789068	0.00004
NM_002474.3(MYH11):c.2785G>T (p.Ala929Ser)	rs906679954	0.00004
NM_002474.3(MYH11):c.301G>A (p.Val101Met)	rs375159635	0.00004
NM_002474.3(MYH11):c.2237C>G (p.Ala746Gly)	rs778651094	0.00003
NM_002474.3(MYH11):c.2659G>A (p.Glu887Lys)	rs201387564	0.00003
NM_002474.3(MYH11):c.3214G>A (p.Ala1072Thr)	rs759155353	0.00002
NM_002474.3(MYH11):c.1576-4A>G	rs189193825	0.00001
NM_002474.3(MYH11):c.1864+8C>T	rs1297078684	0.00001
NM_002474.3(MYH11):c.2098C>T (p.Arg700Trp)	rs886038932	0.00001
NM_002474.3(MYH11):c.2426G>A (p.Arg809Lys)	rs534802983	0.00001
NM_002474.3(MYH11):c.2446A>C (p.Met816Leu)	rs1243566183	0.00001
NM_002474.3(MYH11):c.2476T>C (p.Tyr826His)	rs1436181127	0.00001
NM_002474.3(MYH11):c.3124C>T (p.Arg1042Trp)	rs774490005	0.00001
NM_002474.3(MYH11):c.3152A>G (p.Gln1051Arg)	rs1555557294	0.00001
NM_002474.3(MYH11):c.3233T>C (p.Ile1078Thr)	rs193922629	0.00001
NM_002474.3(MYH11):c.62T>C (p.Ile21Thr)	rs777372840	0.00001
NM_002474.3(MYH11):c.1575+6G>A	rs2041769693
NM_002474.3(MYH11):c.1864+18C>T
NM_002474.3(MYH11):c.2195C>A (p.Ala732Glu)	rs764831521
NM_002474.3(MYH11):c.2747A>G (p.Lys916Arg)	rs1382626826
NM_002474.3(MYH11):c.3115C>G (p.Leu1039Val)	rs1223757069
NM_002474.3(MYH11):c.3654C>G (p.Ala1218=)	rs1555554196
NM_002474.3(MYH11):c.404C>T (p.Ser135Leu)	rs760445629
NM_002474.3(MYH11):c.531-19_531-17del	rs2042478963
NM_002474.3(MYH11):c.809G>C (p.Arg270Pro)
NM_002474.3(MYH11):c.886A>G (p.Arg296Gly)	rs2042214133
NM_002474.3(MYH11):c.95C>G (p.Ala32Gly)

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