Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5879422
DCBLD1
1.000 0.080 6 117463495 intron variant -/GT delins 0.54 1
rs11375254
TP63
0.882 0.080 3 189625454 intergenic variant A/-;AA;AAA;AAAA delins 3
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 4
rs11622887
SYNE3
1.000 0.080 14 95476110 upstream gene variant A/C snv 0.52 2
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 2
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 2
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 11
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs2395655
CDKN1A ; DINOL
0.882 0.120 6 36677919 5 prime UTR variant A/G snv 0.43 0.49 2
rs344924 1.000 0.080 1 67639770 intergenic variant A/G snv 0.17 2
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs10023113
CAMK2D
1.000 0.080 4 113625548 intron variant A/G snv 0.18 1
rs11080466
PIEZO2
1.000 0.080 18 10899030 intron variant A/G snv 0.31 1
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs1950902
MTHFD1
0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 1
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 1
rs2853669
TERT
0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 1
rs3110697
IGFBP3
0.827 0.160 7 45915430 intron variant A/G snv 0.58 1
rs41997
ANKRD7
1.000 0.080 7 118351841 intron variant A/G snv 0.27 1
rs753955
LOC105370113
0.776 0.120 13 23719720 regulatory region variant A/G snv 0.50 1