Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10018951
TRAPPC11
1.000 0.080 4 183688220 intron variant C/T snv 0.18 1
rs10028805
BANK1
0.882 0.160 4 101816093 intron variant G/A snv 0.45 3
rs10032909
LINC01088
1.000 0.080 4 79049054 intron variant A/G snv 0.13 1
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 2
rs10048743
IKZF2
1.000 0.080 2 213025508 intron variant G/T snv 0.78 1
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 16
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 2
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs10245867
JAZF1
0.925 0.080 7 28102567 intron variant G/T snv 0.37 2
rs10276619 1.000 0.080 7 50273756 downstream gene variant G/A snv 0.59 2
rs1028488 1.000 0.080 6 170281387 upstream gene variant G/T snv 0.46 2
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 3
rs1039917
MFHAS1
1.000 0.080 8 8861340 intron variant G/A snv 0.31 1
rs1046089
PRRC2A
0.882 0.200 6 31635190 missense variant G/A snv 0.36 0.40 1
rs10466455
LOC102723568
1.000 0.080 11 34759389 intergenic variant T/C snv 0.39 1
rs1048257
PLD4 ; AHNAK2
1.000 0.080 14 104938047 3 prime UTR variant T/C;G snv 0.54 1
rs10484399 0.851 0.240 6 27566749 intergenic variant A/G snv 5.4E-02 1
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs1049564
PNP
0.882 0.160 14 20472447 missense variant G/A snv 0.19 0.21 2
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 2
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 1
rs10499197 0.925 0.080 6 137811379 intergenic variant T/G snv 2.4E-02 2
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 1
rs1053874
DNASE1 ; TRAP1
0.851 0.240 16 3657746 missense variant G/A;T snv 0.36; 4.0E-06 1