ClinVar Miner

List of variants reported as likely benign for Long QT syndrome 1 by Labcorp Genetics (formerly Invitae), Labcorp

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 171
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_005184.4(CALM3):c.183C>T (p.Asn61=) rs3729761 0.00038
NM_005184.4(CALM3):c.309C>T (p.Ala103=) rs200095251 0.00015
NM_001743.6(CALM2):c.178+12A>G rs376209800 0.00007
NM_005184.4(CALM3):c.237C>T (p.Asp79=) rs147734536 0.00007
NM_005184.4(CALM3):c.444A>T (p.Ala148=) rs779594484 0.00006
NM_001743.6(CALM2):c.348G>A (p.Lys116=) rs546507069 0.00005
NM_001743.6(CALM2):c.421+10T>G rs1193912501 0.00004
NM_001743.6(CALM2):c.4-10C>T rs375578672 0.00003
NM_005184.4(CALM3):c.285+17A>G rs149759804 0.00003
NM_005184.4(CALM3):c.324C>T (p.His108=) rs45587137 0.00003
NM_005184.4(CALM3):c.35-13C>G rs369539598 0.00003
NM_001743.6(CALM2):c.179-15A>G rs747307571 0.00002
NM_001743.6(CALM2):c.285+9A>G rs1687184796 0.00002
NM_001743.6(CALM2):c.421+19C>T rs779412690 0.00002
NM_005184.4(CALM3):c.12G>A (p.Gln4=) rs746427314 0.00002
NM_005184.4(CALM3):c.178+17G>A rs764944151 0.00002
NM_005184.4(CALM3):c.318G>T (p.Leu106=) rs773943649 0.00002
NM_005184.4(CALM3):c.35-10C>T rs748438358 0.00002
NM_005184.4(CALM3):c.354C>T (p.Thr118=) rs750712140 0.00002
NM_001743.6(CALM2):c.123G>A (p.Gly41=) rs369374910 0.00001
NM_001743.6(CALM2):c.165A>G (p.Glu55=) rs1687190320 0.00001
NM_001743.6(CALM2):c.178+17G>A rs934381253 0.00001
NM_001743.6(CALM2):c.178+7C>G rs548280442 0.00001
NM_001743.6(CALM2):c.261A>G (p.Arg87=) rs765564888 0.00001
NM_001743.6(CALM2):c.285+14_285+20del rs1481884663 0.00001
NM_001743.6(CALM2):c.286-14A>T rs1325884656 0.00001
NM_001743.6(CALM2):c.3+20G>T rs1312760543 0.00001
NM_001743.6(CALM2):c.3+9A>C rs749288383 0.00001
NM_001743.6(CALM2):c.336C>T (p.Asn112=) rs751334551 0.00001
NM_001743.6(CALM2):c.35-12T>C rs1309840729 0.00001
NM_001743.6(CALM2):c.417T>C (p.Tyr139=) rs2103823534 0.00001
NM_005184.4(CALM3):c.108G>A (p.Val36=) rs1173698699 0.00001
NM_005184.4(CALM3):c.138A>G (p.Glu46=) rs1454292329 0.00001
NM_005184.4(CALM3):c.147G>A (p.Leu49=) rs760657005 0.00001
NM_005184.4(CALM3):c.165G>A (p.Glu55=) rs764047686 0.00001
NM_005184.4(CALM3):c.178+12A>G rs753670904 0.00001
NM_005184.4(CALM3):c.179-13C>T rs764890178 0.00001
NM_005184.4(CALM3):c.179-18C>T rs761694804 0.00001
NM_005184.4(CALM3):c.24G>A (p.Glu8=) rs1001080500 0.00001
NM_005184.4(CALM3):c.273T>A (p.Arg91=) rs559783307 0.00001
NM_005184.4(CALM3):c.286-10C>G rs375255516 0.00001
NM_005184.4(CALM3):c.286-19C>G rs1478765429 0.00001
NM_005184.4(CALM3):c.286-4C>G rs1471091658 0.00001
NM_005184.4(CALM3):c.3+13G>A rs759824845 0.00001
NM_005184.4(CALM3):c.342G>A (p.Gly114=) rs202189304 0.00001
NM_005184.4(CALM3):c.35-18T>C rs780566686 0.00001
NM_005184.4(CALM3):c.366G>A (p.Val122=) rs1261825623 0.00001
NM_005184.4(CALM3):c.384G>A (p.Glu128=) rs1044212599 0.00001
NM_005184.4(CALM3):c.393C>T (p.Ile131=) rs751608096 0.00001
NM_005184.4(CALM3):c.402T>C (p.Asp134=) rs755022859 0.00001
NM_005184.4(CALM3):c.421+14A>G rs369796184 0.00001
NM_005184.4(CALM3):c.447G>A (p.Lys149=) rs746647108 0.00001
NM_005184.4(CALM3):c.97T>C (p.Leu33=) rs375684773 0.00001
NM_001743.6(CALM2):c.105T>C (p.Thr35=) rs751977184
NM_001743.6(CALM2):c.123G>C (p.Gly41=) rs369374910
NM_001743.6(CALM2):c.178+10C>T rs2465709177
NM_001743.6(CALM2):c.178+10del rs2103825559
NM_001743.6(CALM2):c.178+9T>A rs2465709185
NM_001743.6(CALM2):c.179-15A>T rs747307571
NM_001743.6(CALM2):c.179-29_179-10del rs1558694867
NM_001743.6(CALM2):c.179-8C>G rs1553431791
NM_001743.6(CALM2):c.179-9C>T rs778197988
NM_001743.6(CALM2):c.186C>A (p.Gly62=) rs1573215311
NM_001743.6(CALM2):c.249A>G (p.Glu83=) rs1052083582
NM_001743.6(CALM2):c.282T>C (p.Asp94=)
NM_001743.6(CALM2):c.285+16G>T rs3729963
NM_001743.6(CALM2):c.285+17A>T rs773951686
NM_001743.6(CALM2):c.286-10T>A rs1558694452
NM_001743.6(CALM2):c.286-13A>C rs2465707347
NM_001743.6(CALM2):c.286-14A>G rs1325884656
NM_001743.6(CALM2):c.286-19A>G rs1212624162
NM_001743.6(CALM2):c.286-4C>G
NM_001743.6(CALM2):c.286-4C>T
NM_001743.6(CALM2):c.291C>T (p.Gly97=) rs1011415595
NM_001743.6(CALM2):c.3+11C>G
NM_001743.6(CALM2):c.3+12G>A rs928941745
NM_001743.6(CALM2):c.3+13C>T rs755994751
NM_001743.6(CALM2):c.3+15G>A
NM_001743.6(CALM2):c.3+17G>C rs2465743785
NM_001743.6(CALM2):c.3+18C>G rs1666871767
NM_001743.6(CALM2):c.3+9_3+18del rs1376441280
NM_001743.6(CALM2):c.34+12_34+13delinsCT rs2103844524
NM_001743.6(CALM2):c.34+16C>T
NM_001743.6(CALM2):c.34+17T>C rs2103844496
NM_001743.6(CALM2):c.34+19G>T rs1666638192
NM_001743.6(CALM2):c.342A>C (p.Gly114=) rs2465707182
NM_001743.6(CALM2):c.35-10_35-7del rs757274055
NM_001743.6(CALM2):c.35-14T>C rs1687193279
NM_001743.6(CALM2):c.35-15C>G rs2103825832
NM_001743.6(CALM2):c.4-15T>C rs2465729797
NM_001743.6(CALM2):c.4-17C>G rs1666639561
NM_001743.6(CALM2):c.4-19C>A rs768559585
NM_001743.6(CALM2):c.4-5T>C rs2465729775
NM_001743.6(CALM2):c.4-8C>T
NM_001743.6(CALM2):c.4-8dup rs2103844591
NM_001743.6(CALM2):c.411A>G (p.Val137=) rs1573214087
NM_001743.6(CALM2):c.421+11C>T rs1687162623
NM_001743.6(CALM2):c.421+13G>A rs773732456
NM_001743.6(CALM2):c.421+8T>C rs2465707007
NM_001743.6(CALM2):c.422-12C>T rs751565729
NM_001743.6(CALM2):c.422-12dup rs1326080605
NM_001743.6(CALM2):c.422-13del rs2103821563
NM_001743.6(CALM2):c.422-15C>T rs1278362133
NM_001743.6(CALM2):c.422-15CTT[2] rs775247848
NM_001743.6(CALM2):c.422-17T>C
NM_001743.6(CALM2):c.422-20G>T
NM_001743.6(CALM2):c.422-9C>T rs1391899850
NM_001743.6(CALM2):c.422-9del
NM_001743.6(CALM2):c.429A>G (p.Val143=) rs1400854272
NM_001743.6(CALM2):c.432A>G (p.Gln144=)
NM_001743.6(CALM2):c.57A>G (p.Leu19=) rs754538204
NM_001743.6(CALM2):c.63C>T (p.Asp21=) rs2103825750
NM_005184.4(CALM3):c.132C>T (p.Pro44=) rs2513644456
NM_005184.4(CALM3):c.144G>A (p.Glu48=) rs1599758683
NM_005184.4(CALM3):c.147G>T (p.Leu49=) rs760657005
NM_005184.4(CALM3):c.159C>A (p.Ile53=) rs375106354
NM_005184.4(CALM3):c.159C>T (p.Ile53=) rs375106354
NM_005184.4(CALM3):c.174A>G (p.Ala58=) rs2122245693
NM_005184.4(CALM3):c.178+16C>T
NM_005184.4(CALM3):c.192T>A (p.Ile64=) rs2513644964
NM_005184.4(CALM3):c.213C>T (p.Thr71=) rs1568666350
NM_005184.4(CALM3):c.222C>A (p.Ala74=)
NM_005184.4(CALM3):c.252G>A (p.Glu84=)
NM_005184.4(CALM3):c.27G>A (p.Gln9=) rs1971731867
NM_005184.4(CALM3):c.285+16C>T
NM_005184.4(CALM3):c.286-7C>A
NM_005184.4(CALM3):c.286-8dup rs2122249132
NM_005184.4(CALM3):c.3+11C>T rs2122211406
NM_005184.4(CALM3):c.3+14G>C rs1326371138
NM_005184.4(CALM3):c.3+17G>A rs982176814
NM_005184.4(CALM3):c.3+18G>A rs767873951
NM_005184.4(CALM3):c.3+19T>G rs2065869954
NM_005184.4(CALM3):c.3+20C>T
NM_005184.4(CALM3):c.333G>A (p.Thr111=)
NM_005184.4(CALM3):c.333G>C (p.Thr111=) rs1274089736
NM_005184.4(CALM3):c.339G>C (p.Leu113=) rs143699789
NM_005184.4(CALM3):c.339G>T (p.Leu113=)
NM_005184.4(CALM3):c.34+11T>C rs1971732200
NM_005184.4(CALM3):c.34+16C>T
NM_005184.4(CALM3):c.34+7C>G rs2122231385
NM_005184.4(CALM3):c.35-13C>A rs369539598
NM_005184.4(CALM3):c.35-14C>A rs370430097
NM_005184.4(CALM3):c.35-14C>T rs370430097
NM_005184.4(CALM3):c.35-16C>T
NM_005184.4(CALM3):c.35-18T>G rs780566686
NM_005184.4(CALM3):c.35-19C>T rs757777400
NM_005184.4(CALM3):c.35-9T>C rs1262949304
NM_005184.4(CALM3):c.363G>A (p.Glu121=) rs758692040
NM_005184.4(CALM3):c.387T>C (p.Ala129=) rs1271316314
NM_005184.4(CALM3):c.4-17C>G rs370333318
NM_005184.4(CALM3):c.4-5T>C rs2122231200
NM_005184.4(CALM3):c.4-6T>C rs2513641150
NM_005184.4(CALM3):c.421+10G>T rs2513645953
NM_005184.4(CALM3):c.421+16G>A rs1367034954
NM_005184.4(CALM3):c.421+16G>C
NM_005184.4(CALM3):c.421+16G>T
NM_005184.4(CALM3):c.421+18T>C rs745577081
NM_005184.4(CALM3):c.422-20C>G rs757183576
NM_005184.4(CALM3):c.422-5C>T rs2513646331
NM_005184.4(CALM3):c.422-7T>C rs1971813201
NM_005184.4(CALM3):c.422-7_422-3del
NM_005184.4(CALM3):c.422-8C>T rs1317120997
NM_005184.4(CALM3):c.422-9A>G
NM_005184.4(CALM3):c.429A>G (p.Val143=) rs2122252253
NM_005184.4(CALM3):c.51C>T (p.Phe17=) rs1272522747
NM_005184.4(CALM3):c.57C>A (p.Leu19=) rs1476616729
NM_005184.4(CALM3):c.66G>A (p.Lys22=) rs2122245298
NM_005184.4(CALM3):c.72A>G (p.Gly24=) rs2122245344
NM_005184.4(CALM3):c.75T>C (p.Asp25=) rs2513644344
NM_005184.4(CALM3):c.81T>C (p.Thr27=) rs773251048
NM_005184.4(CALM3):c.9C>T (p.Asp3=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.