ClinVar Miner

List of variants in gene KCNE1 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_000219.6(KCNE1):c.*493C>T rs77190660 0.00371
NM_000219.6(KCNE1):c.-377+13G>A rs41315351 0.00323
NM_000219.6(KCNE1):c.*1338C>T rs74508995 0.00201
NM_000219.6(KCNE1):c.*1556G>A rs886057019 0.00114
NM_000219.6(KCNE1):c.*2001G>A rs41314799 0.00083
NM_000219.6(KCNE1):c.*30C>G rs150963475 0.00061
NM_000219.6(KCNE1):c.*196C>G rs76568182 0.00054
NM_000219.6(KCNE1):c.-334G>A rs891779914 0.00041
NM_000219.6(KCNE1):c.-101A>T rs74706643 0.00038
NM_000219.6(KCNE1):c.-467A>T rs558817846 0.00035
NM_000219.6(KCNE1):c.*1574C>T rs561997378 0.00033
NM_000219.6(KCNE1):c.*373A>G rs41314805 0.00022
NM_000219.6(KCNE1):c.-530G>A rs886057027 0.00019
NM_000219.6(KCNE1):c.*2475A>G rs913676929 0.00017
NM_000219.6(KCNE1):c.*1831C>T rs41314065 0.00016
NM_000219.6(KCNE1):c.111C>T (p.Ser37=) rs150458884 0.00015
NM_000219.6(KCNE1):c.*1447C>G rs886057020 0.00010
NM_000219.6(KCNE1):c.*1859G>A rs754021039 0.00010
NM_000219.6(KCNE1):c.-82T>G rs145416040 0.00010
NM_000219.6(KCNE1):c.-298C>T rs78250687 0.00009
NM_000219.5(KCNE1):c.-605G>A rs780282543 0.00008
NM_000219.6(KCNE1):c.*1290G>A rs890174554 0.00008
NM_000219.6(KCNE1):c.*1832C>T rs886057016 0.00006
NM_000219.6(KCNE1):c.-432G>A rs539503433 0.00005
NM_000219.6(KCNE1):c.-5C>A rs191334763 0.00005
NM_000219.6(KCNE1):c.95G>A (p.Arg32His) rs17857111 0.00005
NM_000219.5(KCNE1):c.-561C>T rs886057028 0.00004
NM_000219.6(KCNE1):c.*457G>A rs886057024 0.00003
NM_000219.6(KCNE1):c.-13C>T rs745925445 0.00003
NM_000219.6(KCNE1):c.-170C>T rs1003872251 0.00002
NM_000219.6(KCNE1):c.-521G>A rs76286526 0.00001
NM_000219.6(KCNE1):c.54G>A (p.Gln18=) rs149875299 0.00001
NM_000219.6(KCNE1):c.*1043T>C rs886057022
NM_000219.6(KCNE1):c.*1078G>A rs41312995
NM_000219.6(KCNE1):c.*1192A>G rs886057021
NM_000219.6(KCNE1):c.*1539C>A rs41314801
NM_000219.6(KCNE1):c.*1542G>A rs1448578468
NM_000219.6(KCNE1):c.*1583A>C rs886057018
NM_000219.6(KCNE1):c.*1701A>G rs886057017
NM_000219.6(KCNE1):c.*1857G>A rs1980726981
NM_000219.6(KCNE1):c.*1928T>C rs886057015
NM_000219.6(KCNE1):c.*2008G>A rs886057011
NM_000219.6(KCNE1):c.*2206G>A rs1454920552
NM_000219.6(KCNE1):c.*2298C>G rs896302148
NM_000219.6(KCNE1):c.*2320G>T rs745512218
NM_000219.6(KCNE1):c.*2329C>A rs373970167
NM_000219.6(KCNE1):c.*2393C>T rs567630448
NM_000219.6(KCNE1):c.*2413T>A rs747442476
NM_000219.6(KCNE1):c.*278A>T rs1980898848
NM_000219.6(KCNE1):c.*366A>C rs1980887753
NM_000219.6(KCNE1):c.*375C>T rs1447216919
NM_000219.6(KCNE1):c.*553A>G rs570907779
NM_000219.6(KCNE1):c.*91del rs748419617
NM_000219.6(KCNE1):c.*960C>T rs544365018
NM_000219.6(KCNE1):c.*995G>C rs886057023
NM_000219.6(KCNE1):c.-225G>C rs886057026
NM_000219.6(KCNE1):c.-24A>G rs1476804491
NM_000219.6(KCNE1):c.-522C>T rs370482882
NM_000219.6(KCNE1):c.-57T>C rs886057025
NM_000219.6(KCNE1):c.347A>C (p.Glu116Ala) rs1235182008

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