ClinVar Miner

Variants in gene AXIN2 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 63
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HGVS dbSNP gnomAD frequency
NM_004655.4(AXIN2):c.2272G>A (p.Ala758Thr) rs145007501 0.00179
NM_004655.4(AXIN2):c.1807G>C (p.Ala603Pro) rs145353986 0.00128
NM_004655.4(AXIN2):c.2428G>A (p.Asp810Asn) rs140344858 0.00123
NM_004655.4(AXIN2):c.2051C>T (p.Ala684Val) rs138287857 0.00112
NM_004655.4(AXIN2):c.1532C>T (p.Thr511Met) rs200883019 0.00109
NM_004655.4(AXIN2):c.1101C>T (p.Pro367=) rs141697521 0.00094
NM_004655.4(AXIN2):c.1985T>C (p.Leu662Pro) rs142476324 0.00084
NM_004655.4(AXIN2):c.1168A>G (p.Ser390Gly) rs139871607 0.00075
NM_004655.4(AXIN2):c.2285G>A (p.Ser762Asn) rs117688560 0.00064
NM_004655.4(AXIN2):c.733C>T (p.Pro245Ser) rs62640028 0.00043
NM_004655.4(AXIN2):c.1685C>T (p.Pro562Leu) rs149764887 0.00031
NM_004655.4(AXIN2):c.203G>A (p.Arg68Gln) rs138056036 0.00020
NM_004655.4(AXIN2):c.1829G>A (p.Arg610Gln) rs376248072 0.00018
NM_004655.4(AXIN2):c.344A>G (p.Asn115Ser) rs370257532 0.00015
NM_004655.4(AXIN2):c.1176G>A (p.Glu392=) rs376052287 0.00014
NM_004655.4(AXIN2):c.1633G>T (p.Gly545Trp) rs148951121 0.00013
NM_004655.4(AXIN2):c.1948C>T (p.Arg650Cys) rs148419444 0.00013
NM_004655.4(AXIN2):c.1882C>T (p.Arg628Trp) rs200201811 0.00011
NM_004655.4(AXIN2):c.2239C>T (p.His747Tyr) rs143571197 0.00008
NM_004655.4(AXIN2):c.475G>T (p.Asp159Tyr) rs753036084 0.00008
NM_004655.4(AXIN2):c.1201-7C>T rs760667639 0.00006
NM_004655.4(AXIN2):c.1267C>T (p.Leu423Phe) rs376630432 0.00006
NM_004655.4(AXIN2):c.1598C>T (p.Ala533Val) rs147716924 0.00006
NM_004655.4(AXIN2):c.623C>T (p.Ala208Val) rs201531372 0.00006
NM_004655.4(AXIN2):c.1222G>A (p.Glu408Lys) rs749846538 0.00004
NM_004655.4(AXIN2):c.1553A>G (p.Tyr518Cys) rs368289818 0.00004
NM_004655.4(AXIN2):c.2216A>G (p.Asn739Ser) rs547630327 0.00004
NM_004655.4(AXIN2):c.2379G>A (p.Glu793=) rs1367633896 0.00004
NM_004655.4(AXIN2):c.1635G>A (p.Gly545=) rs778710067 0.00003
NM_004655.4(AXIN2):c.2196G>A (p.Thr732=) rs878854725 0.00003
NM_004655.4(AXIN2):c.135C>T (p.Val45=) rs376726966 0.00002
NM_004655.4(AXIN2):c.897C>T (p.Asp299=) rs748143308 0.00002
NM_004655.4(AXIN2):c.1284C>A (p.Ser428=) rs750126379 0.00001
NM_004655.4(AXIN2):c.13A>G (p.Met5Val) rs148691166 0.00001
NM_004655.4(AXIN2):c.1494C>T (p.Pro498=) rs1353761854 0.00001
NM_004655.4(AXIN2):c.1510G>C (p.Gly504Arg) rs757512425 0.00001
NM_004655.4(AXIN2):c.1531A>T (p.Thr511Ser) rs376936740 0.00001
NM_004655.4(AXIN2):c.1713C>T (p.Gly571=) rs761978806 0.00001
NM_004655.4(AXIN2):c.1780G>A (p.Ala594Thr) rs876660965 0.00001
NM_004655.4(AXIN2):c.2100C>T (p.Ala700=) rs1057522521 0.00001
NM_004655.4(AXIN2):c.21G>A (p.Val7=) rs1467193033 0.00001
NM_004655.4(AXIN2):c.2405+7G>A rs373593841 0.00001
NM_004655.4(AXIN2):c.2487G>A (p.Pro829=) rs768793839 0.00001
NM_004655.4(AXIN2):c.33G>A (p.Pro11=) rs768626471 0.00001
NM_004655.4(AXIN2):c.414C>T (p.Tyr138=) rs878854730 0.00001
NM_004655.4(AXIN2):c.558C>T (p.Ala186=) rs1598119456 0.00001
NM_004655.4(AXIN2):c.598G>A (p.Val200Met) rs752081909 0.00001
NM_004655.4(AXIN2):c.652C>G (p.Leu218Val) rs766935285 0.00001
NM_004655.4(AXIN2):c.721T>G (p.Cys241Gly) rs370549410 0.00001
NM_004655.4(AXIN2):c.1347C>T (p.Thr449=) rs762279806
NM_004655.4(AXIN2):c.1404CCA[5] (p.His474del) rs570443161
NM_004655.4(AXIN2):c.1404CCA[7] (p.His474dup) rs570443161
NM_004655.4(AXIN2):c.1443C>T (p.Leu481=) rs886053272
NM_004655.4(AXIN2):c.1743C>T (p.Arg581=) rs774932064
NM_004655.4(AXIN2):c.174C>T (p.Asn58=) rs763012548
NM_004655.4(AXIN2):c.1927G>C (p.Ala643Pro) rs748005374
NM_004655.4(AXIN2):c.1952C>G (p.Ser651Trp) rs74006838
NM_004655.4(AXIN2):c.2012G>C (p.Arg671Pro) rs765845684
NM_004655.4(AXIN2):c.2091G>A (p.Leu697=) rs2043915103
NM_004655.4(AXIN2):c.2124G>A (p.Ser708=) rs143243661
NM_004655.4(AXIN2):c.2405+4A>C rs377423720
NM_004655.4(AXIN2):c.339C>T (p.Ala113=) rs1598119867
NM_004655.4(AXIN2):c.629T>C (p.Met210Thr) rs529954883

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