ClinVar Miner

List of variants in gene IGHMBP2 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 87
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HGVS dbSNP gnomAD frequency
NM_002180.3(IGHMBP2):c.2837G>A (p.Arg946Gln) rs149824485 0.00108
NM_002180.3(IGHMBP2):c.767C>G (p.Ala256Gly) rs148095551 0.00065
NM_002180.3(IGHMBP2):c.2176G>A (p.Val726Met) rs143986510 0.00049
NM_002180.3(IGHMBP2):c.2026G>A (p.Gly676Arg) rs149577588 0.00041
NM_002180.3(IGHMBP2):c.832C>G (p.His278Asp) rs144681826 0.00040
NM_002180.3(IGHMBP2):c.1422C>A (p.Asp474Glu) rs61731907 0.00034
NM_002180.3(IGHMBP2):c.1306C>T (p.Arg436Trp) rs138327042 0.00031
NM_002180.3(IGHMBP2):c.2140G>A (p.Gly714Arg) rs146266992 0.00028
NM_002180.3(IGHMBP2):c.2369G>A (p.Arg790Gln) rs147038490 0.00026
NM_002180.3(IGHMBP2):c.2618C>T (p.Pro873Leu) rs141903179 0.00022
NM_002180.3(IGHMBP2):c.1844G>A (p.Arg615His) rs201640213 0.00019
NM_002180.3(IGHMBP2):c.1754A>G (p.Lys585Arg) rs146450269 0.00015
NM_002180.3(IGHMBP2):c.1235+450G>A rs968397154 0.00009
NM_002180.3(IGHMBP2):c.1295C>T (p.Ala432Val) rs370414354 0.00009
NM_002180.3(IGHMBP2):c.2671G>A (p.Val891Ile) rs199614709 0.00009
NM_002180.3(IGHMBP2):c.451G>A (p.Ala151Thr) rs536962342 0.00009
NM_002180.3(IGHMBP2):c.679A>G (p.Ile227Val) rs779639460 0.00009
NM_002180.3(IGHMBP2):c.2612-13G>A rs369494910 0.00008
NM_002180.3(IGHMBP2):c.857G>A (p.Arg286Gln) rs200566598 0.00008
NM_002180.3(IGHMBP2):c.1108G>A (p.Asp370Asn) rs200007067 0.00007
NM_002180.3(IGHMBP2):c.2188C>T (p.Arg730Trp) rs146409569 0.00007
NM_002180.3(IGHMBP2):c.2090C>T (p.Pro697Leu) rs77807333 0.00006
NM_002180.3(IGHMBP2):c.2753G>A (p.Arg918His) rs368584364 0.00006
NM_002180.3(IGHMBP2):c.1913C>T (p.Thr638Met) rs747465472 0.00005
NM_002180.3(IGHMBP2):c.265G>A (p.Val89Met) rs1384314579 0.00005
NM_002180.3(IGHMBP2):c.277G>A (p.Asp93Asn) rs200897747 0.00005
NM_002180.3(IGHMBP2):c.440G>A (p.Arg147Gln) rs138448914 0.00005
NM_002180.3(IGHMBP2):c.761G>A (p.Arg254His) rs761191746 0.00005
NM_002180.3(IGHMBP2):c.2035C>T (p.Arg679Trp) rs371157210 0.00004
NM_002180.3(IGHMBP2):c.2646C>A (p.Asp882Glu) rs372629862 0.00004
NM_002180.3(IGHMBP2):c.856C>T (p.Arg286Trp) rs751421003 0.00004
NM_002180.3(IGHMBP2):c.1342A>G (p.Ile448Val) rs139000973 0.00003
NM_002180.3(IGHMBP2):c.1451C>T (p.Thr484Met) rs1170552394 0.00003
NM_002180.3(IGHMBP2):c.2713G>A (p.Gly905Ser) rs772387164 0.00003
NM_002180.3(IGHMBP2):c.854C>T (p.Ala285Val) rs201188656 0.00003
NM_002180.3(IGHMBP2):c.1766G>T (p.Gly589Val) rs764900781 0.00002
NM_002180.3(IGHMBP2):c.208A>G (p.Arg70Gly) rs563922049 0.00002
NM_002180.3(IGHMBP2):c.2398G>A (p.Gly800Ser) rs751122806 0.00002
NM_002180.3(IGHMBP2):c.284C>T (p.Ala95Val) rs372940951 0.00002
NM_002180.3(IGHMBP2):c.736A>G (p.Ile246Val) rs377678376 0.00002
NM_002180.3(IGHMBP2):c.1036A>G (p.Asn346Asp) rs567322475 0.00001
NM_002180.3(IGHMBP2):c.1106T>A (p.Phe369Tyr) rs756791529 0.00001
NM_002180.3(IGHMBP2):c.1148C>T (p.Ala383Val) rs876661217 0.00001
NM_002180.3(IGHMBP2):c.1442C>G (p.Thr481Arg) rs1555247334 0.00001
NM_002180.3(IGHMBP2):c.167G>A (p.Arg56His) rs571887680 0.00001
NM_002180.3(IGHMBP2):c.1849G>A (p.Val617Ile) rs756289160 0.00001
NM_002180.3(IGHMBP2):c.1874C>T (p.Thr625Ile) rs886048605 0.00001
NM_002180.3(IGHMBP2):c.1933G>A (p.Asp645Asn) rs775138577 0.00001
NM_002180.3(IGHMBP2):c.2123C>G (p.Ser708Cys) rs1042372226 0.00001
NM_002180.3(IGHMBP2):c.2155G>A (p.Gly719Arg) rs1191974842 0.00001
NM_002180.3(IGHMBP2):c.2438C>T (p.Ala813Val) rs779854653 0.00001
NM_002180.3(IGHMBP2):c.2542C>T (p.Pro848Ser) rs1131691275 0.00001
NM_002180.3(IGHMBP2):c.2554G>C (p.Glu852Gln) rs202143060 0.00001
NM_002180.3(IGHMBP2):c.2604A>C (p.Lys868Asn) rs1307749387 0.00001
NM_002180.3(IGHMBP2):c.2649T>G (p.Phe883Leu) rs772539742 0.00001
NM_002180.3(IGHMBP2):c.305C>A (p.Ala102Asp) rs763391719 0.00001
NM_002180.3(IGHMBP2):c.381C>G (p.Ser127Arg) rs775782198 0.00001
NM_002180.3(IGHMBP2):c.657G>T (p.Gly219=) rs879254002 0.00001
NM_002180.3(IGHMBP2):c.830A>G (p.Gln277Arg) rs112495985 0.00001
NM_002180.3(IGHMBP2):c.877G>A (p.Val293Ile) rs761171176 0.00001
NM_002180.3(IGHMBP2):c.905A>G (p.Gln302Arg) rs748286001 0.00001
NM_002180.3(IGHMBP2):c.1031C>T (p.Ser344Leu)
NM_002180.3(IGHMBP2):c.1456G>A (p.Val486Met) rs374456063
NM_002180.3(IGHMBP2):c.1465C>T (p.Leu489Phe) rs1365833591
NM_002180.3(IGHMBP2):c.1511A>G (p.Glu504Gly) rs780426627
NM_002180.3(IGHMBP2):c.1660C>T (p.His554Tyr) rs1859481722
NM_002180.3(IGHMBP2):c.1669C>G (p.Pro557Ala) rs7122089
NM_002180.3(IGHMBP2):c.1789A>T (p.Ile597Phe) rs879253997
NM_002180.3(IGHMBP2):c.184C>T (p.Arg62Trp) rs768631087
NM_002180.3(IGHMBP2):c.2012C>G (p.Thr671Arg) rs377743886
NM_002180.3(IGHMBP2):c.212G>A (p.Arg71Gln)
NM_002180.3(IGHMBP2):c.2133C>G (p.Ser711Arg) rs879254320
NM_002180.3(IGHMBP2):c.2230T>A (p.Leu744Met) rs2154008875
NM_002180.3(IGHMBP2):c.2295C>G (p.His765Gln) rs149185954
NM_002180.3(IGHMBP2):c.2344G>A (p.Val782Met) rs1057523857
NM_002180.3(IGHMBP2):c.2356G>A (p.Ala786Thr)
NM_002180.3(IGHMBP2):c.2429C>T (p.Pro810Leu) rs876661213
NM_002180.3(IGHMBP2):c.2569G>A (p.Gly857Arg) rs1376066801
NM_002180.3(IGHMBP2):c.2573A>G (p.Gln858Arg) rs571303275
NM_002180.3(IGHMBP2):c.2606C>T (p.Ala869Val) rs1353012889
NM_002180.3(IGHMBP2):c.2609A>C (p.Lys870Thr) rs2154008963
NM_002180.3(IGHMBP2):c.2704T>C (p.Cys902Arg) rs1064796817
NM_002180.3(IGHMBP2):c.2755C>A (p.Arg919Ser) rs145945230
NM_002180.3(IGHMBP2):c.455T>C (p.Leu152Pro) rs1858294034
NM_002180.3(IGHMBP2):c.575T>A (p.Leu192Gln) rs879253996
NM_002180.3(IGHMBP2):c.611T>C (p.Leu204Pro)
NM_002180.3(IGHMBP2):c.912+3A>G rs1555244128

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