ClinVar Miner

List of variants in gene combination KLLN, PTEN reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_001126049.2(KLLN):c.-792C>T rs587779982 0.00044
NM_000314.4(PTEN):c.-1242G>A rs587779985 0.00018
NM_001126049.2(KLLN):c.-777C>T rs961642255 0.00013
NM_001126049.2(KLLN):c.-692G>A rs542360599 0.00008
NM_001126049.2(KLLN):c.-780C>T rs876661037 0.00006
NM_001126049.2(KLLN):c.-808G>A rs1487906620 0.00006
NM_001126049.2(KLLN):c.-809T>C rs1189396936 0.00006
NM_001126049.2(KLLN):c.-644A>T rs769351955 0.00005
NM_001126049.2(KLLN):c.-689G>A rs1028896102 0.00004
NM_001126049.2(KLLN):c.-806A>C rs587782761 0.00004
NM_001126049.2(KLLN):c.-846C>T rs1042841710 0.00004
NM_001126049.2(KLLN):c.-675G>A rs1297788990 0.00003
NM_001126049.2(KLLN):c.-760del rs1031612472 0.00003
NM_001126049.2(KLLN):c.-775C>G rs876661005 0.00003
NM_001126049.2(KLLN):c.-803T>A rs587782616 0.00003
NM_001126049.2(KLLN):c.-838T>G rs876661284 0.00003
NM_001126049.2(KLLN):c.-845C>T rs587782068 0.00003
NM_001126049.2(KLLN):c.-742T>G rs954664586 0.00002
NM_001126049.2(KLLN):c.-641C>T rs786204913 0.00001
NM_001126049.2(KLLN):c.-652T>C rs1554889768 0.00001
NM_001126049.2(KLLN):c.-661G>T rs1173886666 0.00001
NM_001126049.2(KLLN):c.-672G>A rs1391231721 0.00001
NM_001126049.2(KLLN):c.-687C>A rs1402112165 0.00001
NM_001126049.2(KLLN):c.-701G>A rs1289454008 0.00001
NM_001126049.2(KLLN):c.-748G>C rs1554889805 0.00001
NM_001126049.2(KLLN):c.-772G>A rs1554889812 0.00001
NM_001126049.2(KLLN):c.-810C>T rs587781548 0.00001
NM_001126049.2(KLLN):c.-829C>T rs1157784032 0.00001
NM_001126049.2(KLLN):c.-870T>C rs1173979974 0.00001
NM_001126049.2(KLLN):c.-647C>T rs1554889767
NM_001126049.2(KLLN):c.-658G>T rs1554889769
NM_001126049.2(KLLN):c.-681A>C rs1554889780
NM_001126049.2(KLLN):c.-684A>T rs1554889784
NM_001126049.2(KLLN):c.-695G>A rs587782034
NM_001126049.2(KLLN):c.-707T>C rs1554889795
NM_001126049.2(KLLN):c.-716G>T rs1042847417
NM_001126049.2(KLLN):c.-733dup rs786204897
NM_001126049.2(KLLN):c.-736G>C rs1554889801
NM_001126049.2(KLLN):c.-748G>A rs1554889805
NM_001126049.2(KLLN):c.-756T>G rs1554889807
NM_001126049.2(KLLN):c.-758G>A rs867484392
NM_001126049.2(KLLN):c.-761C>G rs965758202
NM_001126049.2(KLLN):c.-761C>T rs965758202
NM_001126049.2(KLLN):c.-770C>A rs998222631
NM_001126049.2(KLLN):c.-774G>A rs786204918
NM_001126049.2(KLLN):c.-776G>C rs1554889815
NM_001126049.2(KLLN):c.-790G>A rs1232280343
NM_001126049.2(KLLN):c.-801C>A rs1389966419
NM_001126049.2(KLLN):c.-804_-803delinsAA rs1554889820
NM_001126049.2(KLLN):c.-812G>T rs587779981
NM_001126049.2(KLLN):c.-828C>T rs786203674
NM_001126049.2(KLLN):c.-839C>T rs1443590741
NM_001126049.2(KLLN):c.-840G>T rs563841270
NM_001126049.2(KLLN):c.-841_-840del rs786203981
NM_001126049.2(KLLN):c.-844T>A rs1382791981
NM_001126049.2(KLLN):c.-848_-847insA rs786204886
NM_001126049.2(KLLN):c.-852T>A rs1554889842
NM_001126049.2(KLLN):c.-860G>A rs1554889846
NM_001126049.2(KLLN):c.-861T>A rs876661162
NM_001126049.2(KLLN):c.-862A>G rs1554889848
NM_001126049.2(KLLN):c.-873C>A rs1554889854
NM_001126049.2(KLLN):c.-882A>C rs1554889858
NM_001126049.2(KLLN):c.-882A>G rs1554889858
NM_001126049.2(KLLN):c.-884C>T rs1064793239
NM_001126049.2(KLLN):c.-886C>T rs786204919
NM_001126049.2(KLLN):c.-887C>A rs786204920

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