ClinVar Miner

List of variants in gene MYO3A reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_017433.5(MYO3A):c.-17-79C>T rs17450092 0.04454
NM_017433.5(MYO3A):c.4294-78G>A rs113977717 0.02137
NM_017433.5(MYO3A):c.409-248T>G rs78788833 0.01419
NM_017433.5(MYO3A):c.731+276T>C rs78319880 0.01236
NM_017433.5(MYO3A):c.508+279G>A rs77372144 0.01219
NM_017433.5(MYO3A):c.508+283G>A rs79266743 0.01147
NM_017433.5(MYO3A):c.509-16T>C rs117238740 0.01009
NM_017433.5(MYO3A):c.2999+265G>A rs76099570 0.00997
NM_017433.5(MYO3A):c.4439-254G>A rs185917848 0.00995
NM_017433.5(MYO3A):c.2716-117G>C rs11014972 0.00919
NM_017433.5(MYO3A):c.2114+78A>C rs12256860 0.00917
NM_017433.5(MYO3A):c.4587-30G>T rs115252307 0.00851
NM_017433.5(MYO3A):c.4730+92C>A rs147918803 0.00792
NM_017433.5(MYO3A):c.304-287C>T rs59118546 0.00752
NM_017433.5(MYO3A):c.2417-53T>C rs111849833 0.00646
NM_017433.5(MYO3A):c.2636-276T>A rs146477907 0.00589
NM_017433.5(MYO3A):c.*270A>G rs115859827 0.00498
NM_017433.5(MYO3A):c.2635+55A>G rs74372343 0.00490
NM_017433.5(MYO3A):c.2999+222G>A rs116034089 0.00490
NM_017433.5(MYO3A):c.732-281C>T rs150463218 0.00457
NM_017433.5(MYO3A):c.409-242T>C rs114693840 0.00429
NM_017433.5(MYO3A):c.953+233G>A rs139635391 0.00418
NM_017433.5(MYO3A):c.1777-14G>T rs4592324 0.00409
NM_017433.5(MYO3A):c.3399-102T>C rs148793254 0.00409
NM_017433.5(MYO3A):c.4294-42T>C rs16926632 0.00402
NM_017433.5(MYO3A):c.4730+58C>G rs146767712 0.00373
NM_017433.5(MYO3A):c.3000-311G>A rs76385388 0.00353
NM_017433.5(MYO3A):c.586-258C>T rs147399440 0.00334
NM_017433.5(MYO3A):c.949G>C (p.Ala317Pro) rs61731652 0.00334
NM_017433.5(MYO3A):c.2416+98A>G rs116256511 0.00322
NM_017433.5(MYO3A):c.2999+224C>A rs116319748 0.00291
NM_017433.5(MYO3A):c.508+237G>A rs7911847 0.00291
NM_017433.5(MYO3A):c.4731-39T>G rs139127431 0.00245
NM_017433.5(MYO3A):c.1559C>T (p.Ala520Val) rs72787346 0.00218
NM_017433.5(MYO3A):c.4546-30A>G rs368674587 0.00208
NM_017433.5(MYO3A):c.3111+46G>T rs142382495 0.00148
NM_017433.5(MYO3A):c.4439-12C>T rs201689300 0.00126
NM_017433.5(MYO3A):c.1566A>C (p.Gly522=) rs139121564 0.00100
NM_017433.5(MYO3A):c.177C>T (p.Asp59=) rs139958275 0.00087
NM_017433.5(MYO3A):c.2214T>C (p.Asn738=) rs34803755 0.00084
NM_017433.5(MYO3A):c.546G>T (p.Arg182=) rs148349532 0.00074
NM_017433.5(MYO3A):c.3729G>A (p.Arg1243=) rs146832858 0.00069
NM_017433.5(MYO3A):c.4294-31G>C rs377363591 0.00069
NM_017433.5(MYO3A):c.3398+25C>T rs201812562 0.00048
NM_017433.5(MYO3A):c.3255C>T (p.Ser1085=) rs35541310 0.00041
NM_017433.5(MYO3A):c.4546-168C>T rs144641808 0.00038
NM_017433.5(MYO3A):c.3000-11T>C rs375346333 0.00036
NM_017433.5(MYO3A):c.1248A>G (p.Gln416=) rs143749728 0.00035
NM_017433.5(MYO3A):c.3352A>G (p.Thr1118Ala) rs138955440 0.00035
NM_017433.5(MYO3A):c.797+33A>G rs77216793 0.00028
NM_017433.5(MYO3A):c.2705A>C (p.Asn902Thr) rs142823078 0.00026
NM_017433.5(MYO3A):c.1941A>G (p.Gln647=) rs778345128 0.00023
NM_017433.5(MYO3A):c.1668A>G (p.Leu556=) rs112809849 0.00018
NM_017433.5(MYO3A):c.4530C>T (p.Tyr1510=) rs139504940 0.00016
NM_017433.5(MYO3A):c.906G>A (p.Thr302=) rs139818474 0.00014
NM_017433.5(MYO3A):c.1662-9T>A rs200678745 0.00008
NM_017433.5(MYO3A):c.3027C>T (p.Ser1009=) rs141341808 0.00007
NM_017433.5(MYO3A):c.4242G>A (p.Ser1414=) rs370029963 0.00007
NM_017433.5(MYO3A):c.2376A>G (p.Glu792=) rs758480848 0.00004
NM_017433.5(MYO3A):c.219T>G (p.Ser73=) rs372782893 0.00003
NM_017433.5(MYO3A):c.2703C>A (p.Ile901=) rs201429267 0.00003
NM_017433.5(MYO3A):c.1416C>A (p.Ala472=) rs779845994 0.00001
NM_017433.5(MYO3A):c.3174G>A (p.Lys1058=) rs1172704227 0.00001
NM_017433.5(MYO3A):c.1143T>C (p.Phe381=) rs926365190
NM_017433.5(MYO3A):c.2417-248dup rs10715590
NM_017433.5(MYO3A):c.2635+63G>T rs77096061
NM_017433.5(MYO3A):c.2715+204T>G rs115929922
NM_017433.5(MYO3A):c.3112-197G>A rs117740226
NM_017433.5(MYO3A):c.3585G>T (p.Val1195=) rs372169216
NM_017433.5(MYO3A):c.409-9_409-5del rs770277459
NM_017433.5(MYO3A):c.4438+243del rs144249914
NM_017433.5(MYO3A):c.4567C>G (p.Arg1523Gly) rs727504688
NM_017433.5(MYO3A):c.4731-198C>T rs115874369
NM_017433.5(MYO3A):c.508+36A>T rs75002566
NM_017433.5(MYO3A):c.615C>A (p.Thr205=) rs55634590

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