Gene: KCNQ1 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2237892
rs2237892
KCNQ1
16 0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 0.900 1.000 32 2008 2019
dbSNP: rs2237895
rs2237895
KCNQ1
10 0.790 0.240 11 2835964 intron variant A/C;T snv 0.900 0.889 18 2008 2019
dbSNP: rs2237897
rs2237897
KCNQ1
6 0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 0.880 1.000 11 2008 2019
dbSNP: rs231362
rs231362
KCNQ1 ; KCNQ1OT1
1 1.000 0.080 11 2670241 non coding transcript exon variant A/G snv 0.62 0.840 1.000 10 2010 2019
dbSNP: rs163184
rs163184
KCNQ1
1 1.000 0.080 11 2825839 intron variant T/G snv 0.40 0.810 1.000 8 2010 2018
dbSNP: rs2237896
rs2237896
KCNQ1
1 1.000 0.080 11 2837210 intron variant G/A;T snv 0.810 1.000 6 2011 2019
dbSNP: rs163182
rs163182
KCNQ1
3 0.882 0.160 11 2822986 intron variant G/A;C snv 0.810 1.000 3 2011 2016
dbSNP: rs163177
rs163177
KCNQ1
1 1.000 0.080 11 2817183 intron variant T/C snv 0.45 0.810 1.000 2 2010 2017
dbSNP: rs231361
rs231361
KCNQ1 ; KCNQ1OT1
1 1.000 0.080 11 2670270 non coding transcript exon variant G/A snv 0.31 0.800 1.000 1 2012 2012
dbSNP: rs8181588
rs8181588
KCNQ1
1 1.000 0.080 11 2810311 intron variant T/C snv 0.12 0.800 1.000 1 2014 2014
dbSNP: rs2283228
rs2283228
KCNQ1
1 1.000 0.080 11 2828300 intron variant A/C snv 0.10 0.760 1.000 8 2009 2017
dbSNP: rs163171
rs163171
KCNQ1
1 1.000 0.080 11 2799835 intron variant T/C snv 0.68 0.700 1.000 2 2010 2011
dbSNP: rs234853
rs234853
KCNQ1
1 1.000 0.080 11 2829598 intron variant G/A snv 0.66 0.700 1.000 2 2010 2011
dbSNP: rs117601636
rs117601636
KCNQ1 ; KCNQ1OT1
1 1.000 0.080 11 2620807 non coding transcript exon variant A/G snv 5.5E-03 0.700 1.000 1 2016 2016
dbSNP: rs2237888
rs2237888
KCNQ1
1 1.000 0.080 11 2811675 intron variant C/T snv 0.23 0.700 1.000 1 2011 2011
dbSNP: rs231356
rs231356
KCNQ1 ; KCNQ1OT1
3 0.925 0.080 11 2684113 non coding transcript exon variant A/G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs233449
rs233449
KCNQ1
1 1.000 0.080 11 2822573 intron variant G/A snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs234852
rs234852
KCNQ1
1 1.000 0.080 11 2829552 intron variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs234857
rs234857
KCNQ1
1 1.000 0.080 11 2831299 intron variant T/C snv 0.27 0.700 1.000 1 2011 2011
dbSNP: rs76868685
rs76868685
KCNQ1
1 1.000 0.080 11 2836784 intron variant C/G snv 2.3E-04 0.700 1.000 1 2019 2019
dbSNP: rs77402029
rs77402029
KCNQ1 ; KCNQ1OT1
1 1.000 0.080 11 2619190 non coding transcript exon variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs151290
rs151290
KCNQ1
2 1.000 0.080 11 2800385 intron variant A/C snv 0.67 0.060 0.833 6 2009 2019
dbSNP: rs12576239
rs12576239
KCNQ1
3 1.000 0.080 11 2481089 intron variant C/T snv 0.16 0.010 1.000 1 2017 2017
dbSNP: rs199472698
rs199472698
KCNQ1
2 0.925 0.200 11 2570725 missense variant G/A;C snv 8.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs2074196
rs2074196
KCNQ1
2 1.000 0.080 11 2803570 intron variant G/T snv 8.8E-02 0.010 1.000 1 2009 2009