Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs11127153
PLB1
2 28463094 intron variant T/A;C snv 2
rs11137087 8 7048518 intergenic variant A/G snv 0.60 2
rs111759324 1 101186966 upstream gene variant C/T snv 0.11 2
rs111930700
ACVR1B
12 51967869 intron variant C/G snv 8.4E-02 4
rs11204682
ENSA
1 150623061 intron variant G/A;T snv 4
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs11319879
HHEX
10 92693719 intron variant A/- delins 0.53 2
rs11327184
CCDC26
8 129592027 intron variant C/- delins 0.40 4
rs113422568
SUFU
10 102578181 intron variant G/A snv 0.25 2
rs113473633
NFKB1
1.000 0.040 4 102527974 intron variant A/G snv 1.6E-02 4
rs11353326
ARIH2
3 48941172 intron variant AAAAA/-;A;AA;AAA;AAAA;AAAAAA;AAAAAAA delins 2
rs11359909 3 128603031 intergenic variant G/- delins 0.89 4
rs113604586
ALOX15
17 4639054 missense variant T/C snv 1.7E-03 1.6E-03 2
rs11361923
NOXRED1
14 77396337 intron variant C/- delins 0.54 4
rs113721499 6 31261530 intergenic variant C/T snv 1
rs114050631 2 218156235 regulatory region variant C/T snv 6.9E-03 5
rs114269697
JAK1
1.000 0.040 1 64848529 intron variant C/A snv 7.3E-03 3
rs11428934
CA11 ; SEC1P
19 48640988 intron variant -/G ins 4
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv 5
rs11465296
CCL24
7 75812976 intron variant C/T snv 4.9E-02 2
rs114743735
IRAK2
3 10186296 intron variant C/G snv 4.2E-02 2
rs11555542
ASB2
14 93951185 missense variant T/C snv 3.3E-02 3.7E-02 2
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13