ClinVar Miner

List of variants reported as uncertain significance for Dent disease type 1

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Total variants: 72
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HGVS dbSNP gnomAD frequency
NM_001127898.4(CLCN5):c.*3495A>G rs183523710 0.00296
NM_001127898.4(CLCN5):c.*6217G>A rs781967731 0.00151
NM_001127898.4(CLCN5):c.*2980A>G rs56147923 0.00116
NM_001127898.4(CLCN5):c.*4740C>G rs781970249 0.00102
NM_001127898.4(CLCN5):c.*6240G>C rs782177733 0.00073
NM_001127898.4(CLCN5):c.*6163T>C rs41312128 0.00050
NM_001127898.4(CLCN5):c.*4034A>T rs782274908 0.00042
NM_001127898.4(CLCN5):c.*1292C>T rs781855238 0.00041
NM_001127898.4(CLCN5):c.*2479G>A rs782387568 0.00018
NM_001127898.4(CLCN5):c.*6638G>A rs963123113 0.00014
NM_001127898.4(CLCN5):c.*3091G>A rs782521596 0.00013
NM_001127898.4(CLCN5):c.164-2130C>T rs782456542 0.00012
NM_001127898.4(CLCN5):c.*2324G>A rs782677531 0.00011
NM_001127898.4(CLCN5):c.*4297A>C rs868964422 0.00009
NM_001127898.4(CLCN5):c.*4606A>C rs1024086673 0.00009
NM_001127898.4(CLCN5):c.164-2249C>T rs781792158 0.00009
NM_001127898.4(CLCN5):c.*1874G>A rs1053041096 0.00008
NM_001127898.4(CLCN5):c.*5088G>T rs1024034661 0.00008
NM_001127898.4(CLCN5):c.*2384A>C rs1349157919 0.00007
NM_001127898.4(CLCN5):c.2305G>A (p.Val769Ile) rs201962580 0.00007
NM_001127898.4(CLCN5):c.*5377G>A rs1397080511 0.00006
NM_001127898.4(CLCN5):c.*1339A>G rs782530331 0.00005
NM_001127898.4(CLCN5):c.*1887G>C rs782403661 0.00005
NM_001127898.4(CLCN5):c.*6482C>T rs997377113 0.00005
NM_001127898.4(CLCN5):c.164-2276G>A rs905143179 0.00005
NM_001127898.4(CLCN5):c.*2317G>A rs969354356 0.00004
NM_001127898.4(CLCN5):c.*2460G>A rs111452206 0.00004
NM_001127898.4(CLCN5):c.448C>A (p.His150Asn) rs782412118 0.00004
NM_001127898.4(CLCN5):c.*1625C>T rs1354057843 0.00003
NM_001127898.4(CLCN5):c.*3090C>T rs1057515940 0.00003
NM_001127898.4(CLCN5):c.*3912C>T rs1235435896 0.00003
NM_001127898.4(CLCN5):c.*4911G>A rs1189982201 0.00003
NM_001127898.4(CLCN5):c.*5895T>A rs1057515947 0.00003
NM_001127898.4(CLCN5):c.*6608C>T rs1016988265 0.00003
NM_001127898.4(CLCN5):c.164-2118G>T rs957427726 0.00003
NM_001127898.4(CLCN5):c.*2270A>G rs1057515936 0.00002
NM_001127898.4(CLCN5):c.*2849C>T rs969468804 0.00002
NM_001127898.4(CLCN5):c.*477G>A rs1035298488 0.00002
NM_001127898.4(CLCN5):c.*866A>G rs1323934459 0.00002
NM_001127898.4(CLCN5):c.2342G>C (p.Cys781Ser) rs946613180 0.00002
NM_001127898.4(CLCN5):c.696G>A (p.Ala232=) rs140312372 0.00002
NM_001127898.4(CLCN5):c.*1868T>C rs1934188059 0.00001
NM_001127898.4(CLCN5):c.*1938G>A rs1234577943 0.00001
NM_001127898.4(CLCN5):c.*3627C>T rs1057515941 0.00001
NM_001127898.4(CLCN5):c.*3937C>A rs1057515942 0.00001
NM_001127898.4(CLCN5):c.*39C>T rs781818466 0.00001
NM_001127898.4(CLCN5):c.*5340A>C rs1234568435 0.00001
NM_001127898.4(CLCN5):c.*5844C>T rs957036730 0.00001
NM_001127898.4(CLCN5):c.152G>A (p.Arg51Gln) rs1318459336 0.00001
NM_001127898.4(CLCN5):c.1872G>A (p.Arg624=) rs781948493 0.00001
NM_001127898.4(CLCN5):c.*2557A>G rs1057515938
NM_001127898.4(CLCN5):c.*3071A>G rs1057515939
NM_001127898.4(CLCN5):c.*3388T>G rs1934238784
NM_001127898.4(CLCN5):c.*379G>C rs782172153
NM_001127898.4(CLCN5):c.*3957C>G rs1934256135
NM_001127898.4(CLCN5):c.*504G>C rs1057515931
NM_001127898.4(CLCN5):c.*5240T>C rs1934296250
NM_001127898.4(CLCN5):c.*5815T>C rs1057515945
NM_001127898.4(CLCN5):c.*5970C>T rs1934320534
NM_001127898.4(CLCN5):c.*6694C>T rs1569540841
NM_001127898.4(CLCN5):c.*6841T>C rs1934346410
NM_001127898.4(CLCN5):c.*969A>G rs1057515932
NM_001127898.4(CLCN5):c.1061C>T (p.Ala354Val) rs1060499698
NM_001127898.4(CLCN5):c.1150T>C (p.Trp384Arg)
NM_001127898.4(CLCN5):c.1474G>A (p.Val492Met) rs368039993
NM_001127898.4(CLCN5):c.1495T>C (p.Trp499Arg)
NM_001127898.4(CLCN5):c.1628T>C (p.Met543Thr)
NM_001127898.4(CLCN5):c.1745G>A (p.Gly582Asp)
NM_001127898.4(CLCN5):c.1A>G (p.Met1Val)
NM_001127898.4(CLCN5):c.2293C>T (p.Pro765Ser) rs782267039
NM_001127898.4(CLCN5):c.933+3A>C rs1602123559
NM_001127898.4(CLCN5):c.961G>A (p.Val321Ile) rs1557193807

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