Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs16917667
rs16917667
1.000 0.040 8 95439600 intron variant G/A snv 4.1E-02
CUI: C0018810
Disease: heart rate
heart rate
0.700 1.000 2 2018 2019
dbSNP: rs365990
rs365990
1.000 0.080 14 23392602 missense variant A/G snv 0.34 0.45
CUI: C0018810
Disease: heart rate
heart rate
0.800 1.000 2 2010 2013
dbSNP: rs10002082
rs10002082
4 164159753 intron variant A/G snv 0.20
CUI: C0018810
Disease: heart rate
heart rate
0.700 1.000 1 2018 2018
dbSNP: rs10142635
rs10142635
14 34423401 intron variant A/G snv 3.2E-02
CUI: C0018810
Disease: heart rate
heart rate
0.700 1.000 1 2018 2018
dbSNP: rs1015003
rs1015003
8 37238541 intergenic variant G/T snv 0.58
CUI: C0018810
Disease: heart rate
heart rate
0.800 1.000 1 2013 2013
dbSNP: rs1015451
rs1015451
6 121810339 intergenic variant T/A;C snv
CUI: C0018810
Disease: heart rate
heart rate
0.800 1.000 1 2013 2013
dbSNP: rs10517800
rs10517800
4 164174438 intron variant C/A;T snv
CUI: C0018810
Disease: heart rate
heart rate
0.700 1.000 1 2018 2018
dbSNP: rs11006544
rs11006544
1.000 0.040 10 59510886 intergenic variant T/C snv 7.3E-03
CUI: C0018810
Disease: heart rate
heart rate
0.700 1.000 1 2019 2019
dbSNP: rs11034161
rs11034161
11 37475966 intergenic variant A/C;G snv
CUI: C0018810
Disease: heart rate
heart rate
0.700 1.000 1 2018 2018
dbSNP: rs11065706
rs11065706
12 110717726 downstream gene variant T/C snv 0.19
CUI: C0018810
Disease: heart rate
heart rate
0.800 1.000 1 2013 2013
dbSNP: rs11110004
rs11110004
1.000 0.040 12 99694540 intron variant T/C snv 5.1E-03
CUI: C0018810
Disease: heart rate
heart rate
0.700 1.000 1 2019 2019
dbSNP: rs11118555
rs11118555
1 207767508 non coding transcript exon variant T/A snv 9.3E-02
CUI: C0018810
Disease: heart rate
heart rate
0.800 1.000 1 2013 2013
dbSNP: rs11153730
rs11153730
6 118346359 intergenic variant T/C snv 0.40
CUI: C0018810
Disease: heart rate
heart rate
0.800 1.000 1 2013 2013
dbSNP: rs11154027
rs11154027
1.000 0.080 6 121460244 intergenic variant T/C snv 0.61
CUI: C0018810
Disease: heart rate
heart rate
0.800 1.000 1 2013 2013
dbSNP: rs1120384
rs1120384
4 164161744 intron variant G/A snv 0.16
CUI: C0018810
Disease: heart rate
heart rate
0.700 1.000 1 2018 2018
dbSNP: rs112434206
rs112434206
1.000 0.040 5 33083283 intron variant A/C;G snv 7.6E-03
CUI: C0018810
Disease: heart rate
heart rate
0.700 1.000 1 2019 2019
dbSNP: rs113235453
rs113235453
1.000 0.040 14 31849939 intron variant A/G snv 3.5E-02
CUI: C0018810
Disease: heart rate
heart rate
0.700 1.000 1 2019 2019
dbSNP: rs114821210
rs114821210
1.000 0.040 5 166089843 intergenic variant C/A snv 6.0E-03
CUI: C0018810
Disease: heart rate
heart rate
0.700 1.000 1 2019 2019
dbSNP: rs11578508
rs11578508
1 207955720 upstream gene variant A/G snv 0.29
CUI: C0018810
Disease: heart rate
heart rate
0.800 1.000 1 2013 2013
dbSNP: rs11645781
rs11645781
16 6846127 intron variant A/C;G;T snv
CUI: C0018810
Disease: heart rate
heart rate
0.800 1.000 1 2013 2013
dbSNP: rs11930019
rs11930019
4 164159224 intron variant T/C snv 0.20
CUI: C0018810
Disease: heart rate
heart rate
0.700 1.000 1 2018 2018
dbSNP: rs11931264
rs11931264
4 164160251 intron variant T/C snv 0.20
CUI: C0018810
Disease: heart rate
heart rate
0.700 1.000 1 2018 2018
dbSNP: rs11943491
rs11943491
4 164159378 intron variant G/A snv 0.18
CUI: C0018810
Disease: heart rate
heart rate
0.700 1.000 1 2018 2018
dbSNP: rs12110693
rs12110693
6 121837124 intergenic variant G/A snv 0.23
CUI: C0018810
Disease: heart rate
heart rate
0.700 1.000 1 2009 2009
dbSNP: rs12362161
rs12362161
1.000 0.040 11 98834502 intergenic variant C/A;G snv
CUI: C0018810
Disease: heart rate
heart rate
0.700 1.000 1 2019 2019