Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 1
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs7665090
MANBA
0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 1
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs11191865
STN1
0.925 0.160 10 103913084 intron variant G/A snv 0.44 1
rs2841277
PLD4
0.882 0.120 14 104924668 upstream gene variant C/T snv 0.41 1
rs3827644
ATG5
0.925 0.080 6 106237320 intron variant G/C snv 0.15 1
rs7934606
MUC2
1.000 0.040 11 1100037 intron variant C/G;T snv 1
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 4
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 2
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 2
rs2409781
BLK
0.925 0.120 8 11502048 intron variant T/A;C snv 1
rs624988 0.925 0.120 1 116721168 regulatory region variant T/A;C snv 1
rs35705950 0.763 0.240 11 1219991 splice region variant G/A;T snv 1
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 3
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 2
rs13238352
TNPO3
0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 1
rs13239597
TNPO3 ; TPI1P2
0.882 0.080 7 129055929 non coding transcript exon variant C/A snv 9.0E-02 1
rs4342938 1.000 0.040 10 131557214 intergenic variant A/G snv 0.41 1
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 2