ClinVar Miner

List of variants in gene MYH3 reported as likely benign for not specified

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Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_002470.4(MYH3):c.349-36A>G rs2285467 0.12931
NM_002470.4(MYH3):c.2106C>T (p.Gly702=) rs56259391 0.05968
NM_002470.4(MYH3):c.2610A>G (p.Lys870=) rs56163389 0.05967
NM_002470.4(MYH3):c.5160+30G>T rs73976871 0.03891
NM_002470.4(MYH3):c.5457+3G>A rs200954595 0.02449
NM_002470.4(MYH3):c.6T>C (p.Ser2=) rs17817203 0.02219
NM_002470.4(MYH3):c.3008C>T (p.Ala1003Val) rs34088014 0.02195
NM_002470.4(MYH3):c.4155A>G (p.Glu1385=) rs58343499 0.02173
NM_002470.4(MYH3):c.3938C>T (p.Thr1313Ile) rs35230241 0.02138
NM_002470.4(MYH3):c.5796+29C>G rs570950857 0.01864
NM_002470.4(MYH3):c.4647+27G>A rs73281077 0.01783
NM_002470.4(MYH3):c.4128C>T (p.Tyr1376=) rs112569418 0.01571
NM_002470.4(MYH3):c.699C>T (p.Asn233=) rs16943604 0.01272
NM_002470.4(MYH3):c.349-7C>T rs114366800 0.01261
NM_002470.4(MYH3):c.3009G>A (p.Ala1003=) rs61735353 0.01244
NM_002470.4(MYH3):c.774G>A (p.Lys258=) rs16943598 0.00793
NM_002470.4(MYH3):c.3726T>C (p.Ser1242=) rs77946261 0.00792
NM_002470.4(MYH3):c.3592G>A (p.Ala1198Thr) rs61735358 0.00641
NM_002470.4(MYH3):c.4356+11C>T rs150348272 0.00505
NM_002470.4(MYH3):c.690C>G (p.Ala230=) rs147148934 0.00421
NM_002470.4(MYH3):c.2683-4T>C rs182229640 0.00350
NM_002470.4(MYH3):c.4910C>T (p.Ala1637Val) rs34165480 0.00311
NM_002470.4(MYH3):c.2926-8C>T rs188588330 0.00296
NM_002470.4(MYH3):c.5109G>A (p.Ala1703=) rs114770362 0.00250
NM_002470.4(MYH3):c.3409C>T (p.Arg1137Cys) rs12941197 0.00245
NM_002470.4(MYH3):c.3078C>T (p.Ser1026=) rs146309217 0.00158
NM_002470.4(MYH3):c.2883C>A (p.Thr961=) rs144338240 0.00096
NM_002470.4(MYH3):c.5658+49G>A rs138477550 0.00067
NM_002470.4(MYH3):c.4647+6T>G rs375163919 0.00054
NM_002470.4(MYH3):c.3072C>G (p.Thr1024=) rs139544273 0.00050
NM_002470.4(MYH3):c.208C>T (p.Leu70=) rs779700642 0.00012
NM_002470.4(MYH3):c.505+7T>C rs779225215 0.00008
NM_002470.4(MYH3):c.483C>T (p.Asn161=) rs202066674 0.00005
NM_002470.4(MYH3):c.543C>T (p.Ser181=) rs574573501 0.00004
NM_002470.4(MYH3):c.1446C>T (p.Thr482=) rs200087539 0.00002
NM_002470.4(MYH3):c.3449G>A (p.Arg1150Gln) rs752339755 0.00002
NM_002470.4(MYH3):c.5198C>A (p.Thr1733Lys) rs539740208 0.00002
NM_002470.4(MYH3):c.2083C>A (p.Arg695=) rs767298033
NM_002470.4(MYH3):c.379A>G (p.Asn127Asp) rs797045729
NM_002470.4(MYH3):c.4488T>G (p.Leu1496=) rs886038512
NM_002470.4(MYH3):c.5184G>A (p.Lys1728=)
NM_002470.4(MYH3):c.5254G>A (p.Ala1752Thr) rs34393601
NM_002470.4(MYH3):c.5796+32del rs147333978

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