ClinVar Miner

List of variants in gene MYH7 reported as benign by PreventionGenetics

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Gene type:
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Total variants: 29
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HGVS dbSNP
NM_000257.4(MYH7):c.*20G>A rs45548631
NM_000257.4(MYH7):c.1002C>T (p.Asn334=) rs34803781
NM_000257.4(MYH7):c.1062C>T (p.Gly354=) rs735712
NM_000257.4(MYH7):c.1095G>A (p.Lys365=) rs735711
NM_000257.4(MYH7):c.1128C>T (p.Asp376=) rs2231126
NM_000257.4(MYH7):c.1605A>G (p.Glu535=) rs2069543
NM_000257.4(MYH7):c.1767C>T (p.Asn589=) rs3729816
NM_000257.4(MYH7):c.189C>T (p.Thr63=) rs2069540
NM_000257.4(MYH7):c.2923-18G>A rs7157087
NM_000257.4(MYH7):c.2967T>C (p.Ile989=) rs7157716
NM_000257.4(MYH7):c.3153G>A (p.Ala1051=) rs45540831
NM_000257.4(MYH7):c.3351G>A (p.Glu1117=) rs45554236
NM_000257.4(MYH7):c.3853+21C>T rs45584435
NM_000257.4(MYH7):c.3853+27T>A rs2277475
NM_000257.4(MYH7):c.3853+7C>T rs45467397
NM_000257.4(MYH7):c.3864C>G (p.Ser1288=) rs45501694
NM_000257.4(MYH7):c.3918C>T (p.Leu1306=) rs144420313
NM_000257.4(MYH7):c.3972+15C>T rs3729820
NM_000257.4(MYH7):c.3972+16G>A rs114978322
NM_000257.4(MYH7):c.3973-30A>G rs7159367
NM_000257.4(MYH7):c.4239G>A (p.Ser1413=) rs3729821
NM_000257.4(MYH7):c.480C>T (p.Asn160=) rs45500700
NM_000257.4(MYH7):c.5284-45G>T rs45468101
NM_000257.4(MYH7):c.5655+32G>A rs3729833
NM_000257.4(MYH7):c.597A>G (p.Ala199=) rs2069541
NM_000257.4(MYH7):c.732C>T (p.Phe244=) rs2069542
NM_000257.4(MYH7):c.895+17G>A rs45580436
NM_000257.4(MYH7):c.975C>T (p.Asp325=) rs2231124
NM_000257.4(MYH7):c.999+44T>C rs3729810

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