ClinVar Miner

List of variants reported as likely benign for tooth hard tissue disease

Included ClinVar conditions (36):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_017565.4(FAM20A):c.640+11T>C rs8071830 0.02884
NM_031889.3(ENAM):c.*1500G>A rs72654391 0.02266
NM_031889.3(ENAM):c.*936T>A rs115766831 0.02004
NM_016519.6(AMBN):c.882C>A (p.His294Gln) rs113506649 0.01779
NM_017565.4(FAM20A):c.928+16G>A rs16973042 0.01441
NM_017565.4(FAM20A):c.18G>A (p.Arg6=) rs75228334 0.01179
NM_182758.4(WDR72):c.1839G>A (p.Val613=) rs78493456 0.01140
NM_182758.4(WDR72):c.1437A>C (p.Gln479His) rs34123953 0.01023
NM_031889.3(ENAM):c.177G>T (p.Arg59=) rs2609429 0.01011
NM_031889.3(ENAM):c.1165G>A (p.Gly389Ser) rs74511578 0.01007
NM_182758.4(WDR72):c.857+9A>C rs139139066 0.00974
NM_182758.4(WDR72):c.*588G>A rs140879069 0.00936
NM_182758.4(WDR72):c.*3575T>C rs193055203 0.00834
NM_182758.4(WDR72):c.*3433G>A rs13329257 0.00827
NM_182758.4(WDR72):c.*3325G>A rs74015387 0.00744
NM_004771.4(MMP20):c.415G>A (p.Asp139Asn) rs17099014 0.00724
NM_182758.4(WDR72):c.*3592A>G rs111488180 0.00592
NM_182758.4(WDR72):c.*852G>A rs112576390 0.00577
NM_182758.4(WDR72):c.*2947A>T rs74015388 0.00572
NM_182758.4(WDR72):c.*647G>A rs78618140 0.00478
NM_182758.4(WDR72):c.2598A>G (p.Lys866=) rs115484883 0.00442
NM_182758.4(WDR72):c.*3689A>G rs74871423 0.00094
NM_005220.3(DLX3):c.832G>A (p.Gly278Arg) rs151180891 0.00067
NM_031889.3(ENAM):c.*256G>A rs117342040 0.00061
NM_005220.3(DLX3):c.82G>T (p.Asp28Tyr) rs147702169 0.00058
NM_017565.4(FAM20A):c.1314C>T (p.His438=) rs78050433 0.00053
NM_182758.4(WDR72):c.2942A>G (p.Gln981Arg) rs188590145 0.00053
NM_017565.4(FAM20A):c.513T>C (p.His171=) rs181817943 0.00030
NM_005220.3(DLX3):c.-37C>G rs375929276 0.00029
NM_017565.4(FAM20A):c.43C>T (p.Leu15=) rs372862593 0.00020
NM_017565.4(FAM20A):c.1472C>T (p.Thr491Ile) rs182816928 0.00015
NM_005220.3(DLX3):c.*1328T>G rs568427405 0.00014
NM_017565.4(FAM20A):c.792C>T (p.Ile264=) rs139591838 0.00014
NM_017565.4(FAM20A):c.404+18G>A rs773191671 0.00011
NM_017565.4(FAM20A):c.984T>C (p.Ala328=) rs374633547 0.00011
NM_017565.4(FAM20A):c.321G>C (p.Pro107=) rs568029338 0.00007
NM_017565.4(FAM20A):c.342C>T (p.Asp114=) rs778101746 0.00006
NM_005220.3(DLX3):c.636A>G (p.Ser212=) rs759832786 0.00002
NM_182758.4(WDR72):c.*3734A>G rs371978233 0.00002
NM_005220.3(DLX3):c.465G>A (p.Ala155=) rs534788536
NM_017565.4(FAM20A):c.195C>T (p.Gly65=)
NM_182758.4(WDR72):c.3149-30CT[13] rs57737580
NM_182758.4(WDR72):c.965G>A (p.Arg322His)
NM_198488.5(FAM83H):c.1466del (p.Phe489fs)

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