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: rs2284033
rs2284033
IL2RB
2 0.790 0.160 22 37137994 intron variant G/A snv 0.43 0.810 1.000 3 2010 2012
dbSNP: rs1736135
rs1736135
LOC101927745
4 0.851 0.160 21 15432901 intron variant T/C snv 0.33 0.700 1.000 2 2011 2011
dbSNP: rs4819388
rs4819388
ICOSLG
5 0.790 0.240 21 44227538 3 prime UTR variant T/C snv 0.700 1.000 1 2011 2011
dbSNP: rs762421
rs762421
GATD3A
3 0.851 0.360 21 44195678 intron variant G/A snv 0.700 1.000 1 2011 2011
dbSNP: rs2425656
rs2425656 		1 1.000 0.080 20 44877606 intron variant G/A snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs1061477
rs1061477
KLK3
1 1.000 0.080 19 50856840 intron variant T/C snv 0.42 0.700 1.000 1 2012 2012
dbSNP: rs1229598
rs1229598 		1 1.000 0.080 18 56267556 regulatory region variant A/C;G;T snv 0.700 1.000 1 2000 2000
dbSNP: rs17064520
rs17064520
NEDD4L
1 1.000 0.080 18 58242398 intron variant C/T snv 0.19 0.700 1.000 1 2000 2000
dbSNP: rs17694970
rs17694970
LINC00907
1 1.000 0.080 18 42602641 intron variant A/G snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs1893217
rs1893217
PTPN2
8 0.742 0.440 18 12809341 intron variant A/G snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs2538026
rs2538026 		1 1.000 0.080 18 56261410 intergenic variant A/C;G snv 0.700 1.000 1 2000 2000
dbSNP: rs2542151
rs2542151 		6 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 0.700 1.000 1 2011 2011
dbSNP: rs643507
rs643507
LPIN2 ; CHORDC1P4
1 1.000 0.080 18 2946293 non coding transcript exon variant C/T snv 0.96 0.92 0.700 1.000 1 2013 2013
dbSNP: rs2305480
rs2305480
GSDMB
7 0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 0.860 0.900 4 2008 2018
dbSNP: rs3894194
rs3894194
GSDMA
2 0.882 0.120 17 39965740 missense variant G/A snv 0.46 0.41 0.810 1.000 4 2010 2014
dbSNP: rs7216389
rs7216389
GSDMB
3 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.900 0.889 4 2007 2018
dbSNP: rs2872507
rs2872507 		7 0.752 0.360 17 39884510 intergenic variant G/A;T snv 0.720 1.000 3 2010 2012
dbSNP: rs8079416
rs8079416
LRRC3C
2 0.925 0.080 17 39936460 intron variant T/C snv 0.45 0.710 1.000 3 2010 2012
dbSNP: rs907092
rs907092
IKZF3
3 0.925 0.080 17 39766006 synonymous variant G/A snv 0.41 0.36 0.810 1.000 3 2010 2019
dbSNP: rs11078927
rs11078927
GSDMB
2 0.925 0.080 17 39908152 intron variant C/T snv 0.40 0.35 0.820 1.000 2 2011 2018
dbSNP: rs12150079
rs12150079
ZPBP2
1 0.807 0.280 17 39869164 intron variant G/A snv 0.24 0.700 1.000 2 2010 2011
dbSNP: rs1810132
rs1810132
ERBB2
1 1.000 0.080 17 39709752 intron variant C/T snv 0.64 0.700 1.000 2 2010 2011
dbSNP: rs2271308
rs2271308
STARD3
1 1.000 0.080 17 39661229 non coding transcript exon variant T/C snv 0.61 0.700 1.000 2 2010 2011
dbSNP: rs2290400
rs2290400
GSDMB
6 0.790 0.360 17 39909987 intron variant T/C snv 0.48 0.820 1.000 2 2010 2016
dbSNP: rs4794820
rs4794820
LRRC3C
3 0.790 0.160 17 39933091 intron variant A/G;T snv 0.810 1.000 2 2011 2012