ClinVar Miner

List of variants in gene combination MYH2, MYHAS reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_017534.6(MYH2):c.4329C>T (p.Ala1443=) rs61739663 0.00465
NM_017534.6(MYH2):c.3181C>G (p.Leu1061Val) rs142586585 0.00225
NM_017534.6(MYH2):c.3127T>G (p.Ser1043Ala) rs11658164 0.00123
NM_017534.6(MYH2):c.2062+22G>C rs181799752 0.00106
NM_017534.6(MYH2):c.3048G>A (p.Leu1016=) rs145796634 0.00104
NM_017534.6(MYH2):c.2270T>C (p.Ile757Thr) rs117390537 0.00103
NM_017534.6(MYH2):c.3354+24C>T rs140621687 0.00091
NM_017534.6(MYH2):c.5472+33G>T rs147243814 0.00091
NM_017534.6(MYH2):c.1416+40G>C rs143555593 0.00081
NM_017534.6(MYH2):c.1898-3C>T rs370752980 0.00044
NM_017534.6(MYH2):c.1305C>T (p.Tyr435=) rs539415599 0.00027
NM_017534.6(MYH2):c.2286T>C (p.Tyr762=) rs139196902 0.00016
NM_017534.6(MYH2):c.5577+7C>A rs370883162 0.00014
NM_017534.6(MYH2):c.3459C>T (p.Ser1153=) rs142095822 0.00010
NM_017534.6(MYH2):c.1227C>T (p.Val409=) rs563146441 0.00006
NM_017534.6(MYH2):c.2364C>T (p.Ala788=) rs369107023 0.00004
NM_017534.6(MYH2):c.300T>C (p.Pro100=)
NM_017534.6(MYH2):c.3263+11_3263+15delinsG
NM_017534.6(MYH2):c.3355-4C>G
NM_017534.6(MYH2):c.4007C>A (p.Ala1336Glu) rs138470281
NM_017534.6(MYH2):c.5301+8G>T
NM_017534.6(MYH2):c.5302-7T>C
NM_017534.6(MYH2):c.5805A>T (p.Thr1935=)

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