ClinVar Miner

List of variants in gene MYH9 reported by Eurofins NTD LLC (GA)

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Gene type:
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Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_002473.6(MYH9):c.4876A>G (p.Ile1626Val) rs2269529 0.17342
NM_002473.6(MYH9):c.136C>T (p.Leu46Phe) rs147122501 0.00554
NM_002473.6(MYH9):c.1083C>T (p.Asp361=) rs56001030 0.00436
NM_002473.6(MYH9):c.5143G>A (p.Gly1715Ser) rs148109368 0.00198
NM_002473.6(MYH9):c.4396C>T (p.Arg1466Trp) rs139134727 0.00195
NM_002473.6(MYH9):c.3485+8C>T rs149559551 0.00193
NM_002473.6(MYH9):c.165C>T (p.Ile55=) rs141948797 0.00187
NM_002473.6(MYH9):c.4198C>T (p.Arg1400Trp) rs76368635 0.00123
NM_002473.6(MYH9):c.3192C>T (p.Ile1064=) rs144807538 0.00076
NM_002473.6(MYH9):c.591G>A (p.Ser197=) rs140241271 0.00066
NM_002473.6(MYH9):c.1566G>A (p.Pro522=) rs145517108 0.00054
NM_002473.6(MYH9):c.4878C>T (p.Ile1626=) rs143947828 0.00041
NM_002473.6(MYH9):c.4818G>A (p.Ser1606=) rs202132383 0.00034
NM_002473.6(MYH9):c.1491C>T (p.Ile497=) rs146487404 0.00032
NM_002473.6(MYH9):c.4664A>G (p.Lys1555Arg) rs141543499 0.00027
NM_002473.6(MYH9):c.1479G>A (p.Gln493=) rs376262583 0.00025
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.4024C>T (p.Arg1342Trp) rs147901502 0.00014
NM_002473.6(MYH9):c.5185G>T (p.Ala1729Ser) rs140662138 0.00013
NM_002473.6(MYH9):c.5151-4G>A rs368125656 0.00007
NM_002473.6(MYH9):c.3213C>T (p.Ile1071=) rs552133535 0.00005
NM_002473.6(MYH9):c.3214G>A (p.Ala1072Thr) rs532156048 0.00004
NM_002473.6(MYH9):c.4150G>C (p.Glu1384Gln) rs200616409 0.00004
NM_002473.6(MYH9):c.108C>T (p.Ser36=) rs764743124 0.00002
NM_002473.6(MYH9):c.3591C>T (p.Ala1197=) rs549408462 0.00002
NM_002473.6(MYH9):c.5151-5C>T rs762613036 0.00001
NM_002473.6(MYH9):c.4303A>G (p.Ser1435Gly) rs1569534912
NM_002473.6(MYH9):c.5174G>A (p.Arg1725Gln) rs993895986
NM_002473.6(MYH9):c.5175G>A (p.Arg1725=) rs896873577
NM_002473.6(MYH9):c.5275-10del rs552643559

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