ClinVar Miner

List of variants in gene combination MYH2, MYHAS reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_017534.6(MYH2):c.5176-272C>T rs115404283 0.01394
NM_017534.6(MYH2):c.3872-123G>A rs75608430 0.01352
NM_017534.6(MYH2):c.5674-10T>C rs16943488 0.01190
NM_017534.6(MYH2):c.349-82T>C rs139287914 0.01133
NM_017534.6(MYH2):c.506-299G>A rs73974760 0.01101
NM_017534.6(MYH2):c.2697+101A>T rs138017232 0.00863
NM_017534.6(MYH2):c.505+25del rs375322854 0.00681
NM_017534.6(MYH2):c.5577+60T>G rs143769476 0.00647
NM_017534.6(MYH2):c.4188-285T>C rs77361283 0.00565
NM_017534.6(MYH2):c.1897+257T>C rs9903572 0.00558
NM_017534.6(MYH2):c.5673+179A>G rs114087730 0.00557
NM_017534.6(MYH2):c.1898-132T>C rs9903038 0.00550
NM_017534.6(MYH2):c.904+215A>G rs114395943 0.00514
NM_017534.6(MYH2):c.1974+167G>A rs9895977 0.00503
NM_017534.6(MYH2):c.506-26T>C rs9903455 0.00494
NM_017534.6(MYH2):c.4329C>T (p.Ala1443=) rs61739663 0.00450
NM_017534.6(MYH2):c.5780G>A (p.Arg1927Gln) rs34161789 0.00444
NM_017534.6(MYH2):c.4187+239C>T rs73974757 0.00408
NM_017534.6(MYH2):c.1974+110T>C rs138088239 0.00371
NM_017534.6(MYH2):c.3745-173G>A rs865823276 0.00371
NM_017534.6(MYH2):c.5674-26C>G rs141450971 0.00370
NM_017534.6(MYH2):c.5175+162T>C rs186562411 0.00343
NM_017534.6(MYH2):c.2295G>A (p.Gly765=) rs79757188 0.00317
NM_017534.6(MYH2):c.1417-285T>G rs189072407 0.00262
NM_017534.6(MYH2):c.3181C>G (p.Leu1061Val) rs142586585 0.00221
NM_017534.6(MYH2):c.2698-8A>C rs186620412 0.00206
NM_017534.6(MYH2):c.*51C>A rs2286357 0.00127
NM_017534.6(MYH2):c.3127T>G (p.Ser1043Ala) rs11658164 0.00123
NM_017534.6(MYH2):c.3048G>A (p.Leu1016=) rs145796634 0.00112
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.87T>C (p.Asn29=) rs148217318 0.00048
NM_017534.6(MYH2):c.2062+8A>G rs117562194 0.00039
NM_017534.6(MYH2):c.4258C>T (p.Leu1420Phe) rs187438258 0.00019
NM_017534.6(MYH2):c.4304T>C (p.Met1435Thr) rs139691540 0.00019
NM_017534.6(MYH2):c.4149G>A (p.Thr1383=) rs376738763 0.00008
NM_017534.6(MYH2):c.3384C>T (p.Ile1128=) rs139130605 0.00007
NM_017534.6(MYH2):c.1008+222dup rs56139789
NM_017534.6(MYH2):c.2181-294C>G rs9891328
NM_017534.6(MYH2):c.3355-31A>C rs147207041
NM_017534.6(MYH2):c.3745-188_3745-186dup rs71365770
NM_017534.6(MYH2):c.5674-178GT[8] rs374726017

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