Source: GWASCAT ×
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: rs3802842
rs3802842
COLCA2 ; COLCA1
9 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.700 1.000 8 2008 2019
dbSNP: rs7229639
rs7229639
SMAD7
9 0.763 0.080 18 48924606 intron variant A/G snv 0.87 0.700 1.000 5 2014 2019
dbSNP: rs10774214
rs10774214
CCND2-AS1
9 0.790 0.080 12 4259186 intron variant T/C snv 0.54 0.700 1.000 4 2013 2019
dbSNP: rs10795668
rs10795668
LOC105376400
9 0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 0.700 1.000 4 2008 2019
dbSNP: rs11196172
rs11196172
TCF7L2
9 0.708 0.200 10 112967084 intron variant G/A snv 0.13 0.700 1.000 4 2014 2019
dbSNP: rs2423279
rs2423279 		9 0.790 0.080 20 7831703 downstream gene variant T/C snv 0.29 0.700 1.000 4 2013 2019
dbSNP: rs3824999
rs3824999
POLD3
9 0.790 0.080 11 74634505 intron variant T/G snv 0.40 0.700 1.000 4 2012 2019
dbSNP: rs4779584
rs4779584 		9 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 0.700 1.000 4 2008 2015
dbSNP: rs647161
rs647161
C5orf66
9 0.776 0.080 5 135163402 intron variant C/A snv 0.63 0.700 1.000 4 2013 2019
dbSNP: rs961253
rs961253 		9 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 0.700 1.000 4 2008 2019
dbSNP: rs10411210
rs10411210
RHPN2
9 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.700 1.000 3 2008 2019
dbSNP: rs12241008
rs12241008
VTI1A
9 0.716 0.160 10 112520943 intron variant T/C snv 0.13 0.700 1.000 3 2014 2019
dbSNP: rs2427308
rs2427308
CABLES2
9 0.790 0.080 20 62394395 intron variant C/T snv 0.22 0.700 1.000 3 2014 2019
dbSNP: rs2450115
rs2450115
LOC105375712
9 0.790 0.080 8 116611854 intergenic variant T/C snv 0.19 0.700 1.000 3 2016 2019
dbSNP: rs4444235
rs4444235 		9 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.700 1.000 3 2008 2019
dbSNP: rs6469656
rs6469656 		9 0.790 0.080 8 116635549 regulatory region variant G/A;C snv 0.700 1.000 3 2014 2019
dbSNP: rs7014346
rs7014346
POU5F1B ; CASC8 ; PCAT1
9 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.700 1.000 3 2008 2016
dbSNP: rs73376930
rs73376930
GREM1 ; LOC100131315
9 0.790 0.080 15 32720301 intron variant A/G snv 0.25 0.700 1.000 3 2014 2019
dbSNP: rs1035209
rs1035209 		9 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 0.700 1.000 2 2014 2019
dbSNP: rs10849432
rs10849432
LOC105369625
9 0.790 0.080 12 6276561 intergenic variant C/T snv 0.84 0.700 1.000 2 2014 2016
dbSNP: rs10911251
rs10911251
LAMC1
9 0.790 0.080 1 183112059 intron variant A/C snv 0.37 0.700 1.000 2 2013 2019
dbSNP: rs12412391
rs12412391
LINC01475
9 0.790 0.080 10 99529178 intron variant A/G;T snv 0.700 1.000 2 2014 2016
dbSNP: rs12603526
rs12603526
NXN
9 0.790 0.080 17 897353 intron variant T/C snv 2.3E-02 0.700 1.000 2 2014 2016
dbSNP: rs1810502
rs1810502 		9 0.790 0.080 20 50440951 intergenic variant C/T snv 0.49 0.700 1.000 2 2019 2019
dbSNP: rs35360328
rs35360328 		9 0.790 0.080 3 40883471 intergenic variant T/A snv 0.11 0.700 1.000 2 2015 2019