ClinVar Miner

List of variants reported as likely benign for autosomal dominant nonsyndromic hearing loss 17 by Illumina Laboratory Services, Illumina

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_002473.6(MYH9):c.*1329C>T rs146582828 0.00786
NM_002473.6(MYH9):c.*686C>T rs55994070 0.00779
NM_002473.6(MYH9):c.*81C>T rs56134611 0.00569
NM_002473.6(MYH9):c.136C>T (p.Leu46Phe) rs147122501 0.00554
NM_002473.6(MYH9):c.7C>G (p.Gln3Glu) rs56200894 0.00231
NM_002473.6(MYH9):c.5143G>A (p.Gly1715Ser) rs148109368 0.00198
NM_002473.6(MYH9):c.4396C>T (p.Arg1466Trp) rs139134727 0.00195
NM_002473.6(MYH9):c.4952T>C (p.Met1651Thr) rs142094977 0.00165
NM_002473.6(MYH9):c.5818G>A (p.Gly1940Arg) rs140588099 0.00156
NM_002473.6(MYH9):c.705+14C>T rs142552338 0.00139
NM_002473.6(MYH9):c.5323A>G (p.Lys1775Glu) rs145139708 0.00134
NM_002473.6(MYH9):c.4198C>T (p.Arg1400Trp) rs76368635 0.00123
NM_002473.6(MYH9):c.1176G>A (p.Pro392=) rs143316848 0.00121
NM_002473.6(MYH9):c.1158C>T (p.Thr386=) rs138502859 0.00119
NM_002473.6(MYH9):c.705+11C>T rs201738304 0.00114
NM_002473.6(MYH9):c.2448C>T (p.Cys816=) rs113285582 0.00112
NM_002473.6(MYH9):c.-19-7C>T rs184332718 0.00111
NM_002473.6(MYH9):c.4727G>A (p.Arg1576Gln) rs143269195 0.00088
NM_002473.6(MYH9):c.5010G>A (p.Glu1670=) rs76069100 0.00088
NM_002473.6(MYH9):c.615C>T (p.Gly205=) rs139466141 0.00088
NM_002473.6(MYH9):c.1242C>T (p.Ile414=) rs138436678 0.00083
NM_002473.6(MYH9):c.*8C>T rs201455315 0.00081
NM_002473.6(MYH9):c.3192C>T (p.Ile1064=) rs144807538 0.00076
NM_002473.6(MYH9):c.2872G>A (p.Ala958Thr) rs151036570 0.00066
NM_002473.6(MYH9):c.5877C>T (p.Ala1959=) rs144179406 0.00066
NM_002473.6(MYH9):c.4344+10C>T rs200977419 0.00061
NM_002473.6(MYH9):c.3216G>A (p.Ala1072=) rs139441456 0.00055
NM_002473.6(MYH9):c.5026A>G (p.Lys1676Glu) rs138158369 0.00046
NM_002473.6(MYH9):c.3340T>C (p.Ser1114Pro) rs200901330 0.00044
NM_002473.6(MYH9):c.4878C>T (p.Ile1626=) rs143947828 0.00041
NM_002473.6(MYH9):c.769+15C>T rs201691359 0.00039
NM_002473.6(MYH9):c.5765+9C>T rs201008102 0.00038
NM_002473.6(MYH9):c.*329C>T rs566336121 0.00035
NM_002473.6(MYH9):c.2500-14A>G rs199505086 0.00031
NM_002473.6(MYH9):c.4359G>A (p.Glu1453=) rs202127454 0.00028
NM_002473.6(MYH9):c.*325C>T rs189775203 0.00026
NM_002473.6(MYH9):c.1479G>A (p.Gln493=) rs376262583 0.00025
NM_002473.6(MYH9):c.2061C>T (p.Leu687=) rs143801000 0.00022
NM_002473.6(MYH9):c.4956C>T (p.Arg1652=) rs148632964 0.00016
NM_002473.6(MYH9):c.2295C>T (p.Ala765=) rs150133983 0.00015
NM_002473.6(MYH9):c.32A>G (p.Tyr11Cys) rs201415443 0.00015
NM_002473.6(MYH9):c.5709C>T (p.Ala1903=) rs145444485 0.00012
NM_002473.6(MYH9):c.2635A>C (p.Met879Leu) rs200328859 0.00005
NM_002473.6(MYH9):c.933C>T (p.Pro311=) rs202045249 0.00005
NM_002473.6(MYH9):c.3320G>A (p.Arg1107Gln) rs137924205 0.00004
NM_002473.6(MYH9):c.3606G>A (p.Ala1202=) rs771461880 0.00003
NM_002473.6(MYH9):c.318C>T (p.Tyr106=) rs202117532 0.00002
NM_002473.6(MYH9):c.2217G>C (p.Ala739=) rs756586731

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