Source: GWASDB

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: rs13117307
rs13117307
0.827 0.080 4 55885574 intron variant C/T snv 0.21
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.730 1.000 1 2013 2017
dbSNP: rs4282438
rs4282438
0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.730 1.000 1 2013 2016
dbSNP: rs2516448
rs2516448
0.827 0.120 6 31422633 intron variant T/C;G snv
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.720 1.000 1 2013 2016
dbSNP: rs3117027
rs3117027
0.882 0.080 6 33121846 intron variant C/A;G snv
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.720 1.000 1 2013 2018
dbSNP: rs8067378
rs8067378
0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.720 1.000 1 2013 2017
dbSNP: rs9272143
rs9272143
0.882 0.080 6 32633026 intron variant T/C snv 0.49
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.720 1.000 1 2013 2014
dbSNP: rs9277535
rs9277535
0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.720 1.000 1 2013 2018
dbSNP: rs9277952
rs9277952
0.851 0.080 6 33236497 upstream gene variant G/A snv 0.10
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.720 1.000 1 2013 2016
dbSNP: rs2116260
rs2116260
1.000 0.080 6 33057663 TF binding site variant T/C snv 8.6E-02
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.700 1.000 1 2013 2013
dbSNP: rs213210
rs213210
0.742 0.240 6 33208047 upstream gene variant A/C;G snv
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.700 1.000 1 2013 2013
dbSNP: rs3117008
rs3117008
1.000 0.080 6 33128497 intron variant G/A snv 0.43
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.700 1.000 1 2013 2013
dbSNP: rs3117039
rs3117039
0.925 0.160 6 33118074 intron variant C/T snv 0.35
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.700 1.000 1 2013 2013
dbSNP: rs3129275
rs3129275
1.000 0.080 6 33126481 intron variant C/T snv 0.40
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.700 1.000 1 2013 2013
dbSNP: rs4713607
rs4713607
1.000 0.080 6 33123059 intron variant G/A snv 0.43
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.700 1.000 1 2013 2013
dbSNP: rs7770370
rs7770370
0.925 0.160 6 33081144 non coding transcript exon variant A/G snv 0.27
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.700 1.000 1 2013 2013
dbSNP: rs9391756
rs9391756
1.000 0.080 6 33148017 upstream gene variant C/A;T snv
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.700 1.000 1 2013 2013
dbSNP: rs997363
rs997363
0.925 0.080 2 227644742 intron variant C/T snv 0.64
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.700 1.000 1 2014 2014