ClinVar Miner

List of variants reported as benign for Parietal foramina 2

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ClinVar version:
Total variants: 73
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HGVS dbSNP gnomAD frequency
NM_021926.4(ALX4):c.621A>G (p.Ser207=) rs10769028 0.99242
NM_021926.4(ALX4):c.*2110A>G rs7105993 0.99108
NM_021926.4(ALX4):c.467-45T>C rs11037929 0.95917
NM_021926.4(ALX4):c.*3107A>G rs4755239 0.90297
NM_021926.4(ALX4):c.*547A>G rs4755796 0.81277
NM_021926.4(ALX4):c.778-117T>C rs10742699 0.79676
NM_021926.4(ALX4):c.*2682C>T rs897005 0.69471
NM_021926.4(ALX4):c.*517C>T rs4755797 0.67187
NM_021926.4(ALX4):c.778-140G>C rs10769024 0.57195
NM_021926.4(ALX4):c.104G>C (p.Arg35Thr) rs3824915 0.42227
NM_021926.4(ALX4):c.304C>T (p.Pro102Ser) rs12421995 0.32933
NM_021926.4(ALX4):c.1074C>T (p.His358=) rs3802805 0.29957
NM_021926.4(ALX4):c.*2479T>C rs897004 0.26076
NM_021926.4(ALX4):c.*2832A>C rs1840254 0.24185
NM_021926.4(ALX4):c.*3166C>T rs7116335 0.23498
NM_021926.4(ALX4):c.*228C>T rs4755798 0.23484
NM_021926.4(ALX4):c.729G>A (p.Ala243=) rs11037928 0.10227
NM_021926.4(ALX4):c.879C>T (p.Leu293=) rs12419361 0.09492
NM_021926.4(ALX4):c.*1896A>G rs55959427 0.08833
NM_021926.4(ALX4):c.*1699G>T rs7942612 0.08488
NM_021926.4(ALX4):c.778-11G>A rs75147697 0.08417
NM_021926.4(ALX4):c.*973G>A rs117526668 0.07512
NM_021926.4(ALX4):c.*1447G>A rs11037920 0.02530
NM_021926.4(ALX4):c.594C>A (p.Leu198=) rs61737295 0.02470
NM_021926.4(ALX4):c.*2226G>A rs78607024 0.02447
NM_021926.4(ALX4):c.*972C>T rs151214135 0.01593
NM_021926.4(ALX4):c.*3596C>G rs11037919 0.01480
NM_021926.4(ALX4):c.*1901A>G rs78007447 0.01238
NM_021926.4(ALX4):c.*922T>G rs185632337 0.01097
NM_021926.4(ALX4):c.*923C>T rs181642223 0.01096
NM_021926.4(ALX4):c.*1227G>A rs76501131 0.01081
NM_021926.4(ALX4):c.*902G>A rs76229477 0.00875
NM_021926.4(ALX4):c.*1713G>C rs76845793 0.00799
NM_021926.4(ALX4):c.*156G>A rs376658247 0.00776
NM_021926.4(ALX4):c.63C>T (p.Tyr21=) rs61737298 0.00736
NM_021926.4(ALX4):c.918G>A (p.Pro306=) rs145904583 0.00731
NM_021926.4(ALX4):c.*1345G>A rs113781536 0.00680
NM_021926.4(ALX4):c.*3012C>G rs117877500 0.00663
NM_021926.4(ALX4):c.*2507G>A rs75369525 0.00635
NM_021926.4(ALX4):c.*1131T>C rs10458913 0.00627
NM_021926.4(ALX4):c.*266T>G rs60998360 0.00609
NM_021926.4(ALX4):c.69G>C (p.Pro23=) rs115968657 0.00532
NM_021926.4(ALX4):c.*2828C>T rs77015141 0.00418
NM_021926.4(ALX4):c.*3769T>C rs116662493 0.00400
NM_021926.4(ALX4):c.*3773A>G rs114755169 0.00394
NM_021926.4(ALX4):c.*2244G>A rs183882854 0.00303
NM_021926.4(ALX4):c.*997C>G rs192668810 0.00293
NM_021926.4(ALX4):c.*2673T>A rs146304390 0.00260
NM_021926.4(ALX4):c.*963G>A rs140400459 0.00249
NM_021926.4(ALX4):c.*524C>T rs534068592 0.00212
NM_021926.4(ALX4):c.*1913G>A rs189662898 0.00188
NM_021926.4(ALX4):c.*46G>A rs72905941 0.00185
NM_021926.4(ALX4):c.*262G>A rs560751940 0.00180
NM_021926.4(ALX4):c.*3123G>A rs182987016 0.00175
NM_021926.4(ALX4):c.*1629C>T rs184605209 0.00172
NM_021926.4(ALX4):c.*2845G>A rs182853569 0.00172
NM_021926.4(ALX4):c.*1048C>T rs532888348 0.00153
NM_021926.4(ALX4):c.*1088G>A rs149094042 0.00135
NM_021926.4(ALX4):c.*782A>G rs373562733 0.00123
NM_021926.4(ALX4):c.*1121C>T rs146483327 0.00118
NM_021926.4(ALX4):c.*1365C>A rs529798397 0.00041
NM_021926.4(ALX4):c.*4105C>T rs560087261 0.00040
NM_021926.4(ALX4):c.*2750G>A rs372769669 0.00029
NM_021926.4(ALX4):c.226C>A (p.Pro76Thr) rs79200219 0.00018
NM_021926.4(ALX4):c.-36G>C rs533107251 0.00012
NM_021926.4(ALX4):c.*3999C>T rs369328027 0.00011
NM_021926.4(ALX4):c.*437C>T rs542591808 0.00006
NM_021926.4(ALX4):c.1106G>A (p.Gly369Glu) rs750221052 0.00006
NM_021926.4(ALX4):c.474G>C (p.Glu158Asp) rs553689111 0.00001
NM_021926.4(ALX4):c.*1532G>A rs373805569
NM_021926.4(ALX4):c.*3081C>T rs139681611
NM_021926.4(ALX4):c.*3405G>A rs7115841
NM_021926.4(ALX4):c.*944G>T rs188954464

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