Source: GWASDB ×
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: rs10488631
rs10488631
TNPO3
7 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 0.800 1.000 4 2009 2015
dbSNP: rs3790567
rs3790567
IL12RB2
1 0.851 0.240 1 67356694 intron variant A/G snv 0.61 0.800 1.000 2 2009 2010
dbSNP: rs6441286
rs6441286
IL12A-AS1
1 0.925 0.080 3 160011091 intron variant T/G snv 0.36 0.800 1.000 2 2009 2010
dbSNP: rs2395148
rs2395148
TSBP1 ; TSBP1-AS1
2 0.882 0.200 6 32353777 intron variant G/T snv 4.6E-02 0.800 1.000 1 2009 2009
dbSNP: rs2856683
rs2856683 		4 0.827 0.320 6 32687441 regulatory region variant T/A;C;G snv 0.25 0.800 1.000 1 2009 2009
dbSNP: rs3135363
rs3135363 		4 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 0.800 1.000 1 2009 2009
dbSNP: rs4679904
rs4679904 		1 0.925 0.080 3 160623108 intergenic variant C/G;T snv 0.800 1.000 1 2009 2009
dbSNP: rs9357152
rs9357152 		4 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 0.800 1.000 1 2009 2009
dbSNP: rs7774434
rs7774434 		5 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 0.800 1.000 3 2010 2015
dbSNP: rs9303277
rs9303277
IKZF3
4 0.790 0.240 17 39820216 intron variant C/T snv 0.52 0.800 1.000 3 2010 2017
dbSNP: rs3745516
rs3745516
SPIB
1 0.925 0.080 19 50423485 intron variant A/G snv 0.62 0.800 1.000 2 2010 2015
dbSNP: rs2293370
rs2293370
TIMMDC1
2 0.882 0.160 3 119501087 intron variant G/A snv 0.18 0.810 1.000 4 2011 2019
dbSNP: rs1054037
rs1054037
MANBA
1 1.000 0.080 4 102631552 3 prime UTR variant C/A;T snv 0.800 1.000 2 2011 2015
dbSNP: rs12924729
rs12924729
CLEC16A
2 0.882 0.200 16 11093926 intron variant G/A snv 0.34 0.800 1.000 2 2011 2015
dbSNP: rs12935413
rs12935413
CLEC16A
1 1.000 0.080 16 11116590 intron variant G/A snv 0.34 0.700 1.000 2 2011 2012
dbSNP: rs1800693
rs1800693
TNFRSF1A
2 0.776 0.360 12 6330843 non coding transcript exon variant T/C snv 0.36; 4.0E-06 0.38 0.800 1.000 2 2011 2015
dbSNP: rs2866413
rs2866413
MANBA
1 1.000 0.080 4 102635920 missense variant G/A;C snv 0.54; 2.4E-05 0.700 1.000 2 2011 2012
dbSNP: rs4149581
rs4149581
TNFRSF1A
1 1.000 0.080 12 6337819 intron variant T/A;C snv 0.700 1.000 2 2011 2012
dbSNP: rs485499
rs485499
LINC01100 ; IL12A-AS1
1 0.925 0.080 3 160028076 intron variant T/C snv 0.29 0.800 1.000 2 2011 2015
dbSNP: rs4938573
rs4938573 		2 0.851 0.280 11 118871133 regulatory region variant C/T snv 0.79 0.700 1.000 2 2011 2012
dbSNP: rs6897932
rs6897932
IL7R
2 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 0.800 1.000 2 2011 2017
dbSNP: rs7665090
rs7665090
MANBA
1 0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 0.800 1.000 2 2011 2012
dbSNP: rs911263
rs911263
RAD51B
1 0.851 0.200 14 68286876 intron variant C/T snv 0.57 0.800 1.000 2 2011 2015
dbSNP: rs1003643
rs1003643 		1 1.000 0.080 22 39280489 downstream gene variant T/G snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs1003644
rs1003644 		1 1.000 0.080 22 39280739 downstream gene variant G/A snv 0.31 0.700 1.000 1 2011 2011