Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 3
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 2
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 4
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 4
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 1
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 2
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 2
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 2
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 2
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 1
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 4
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 3
rs2073618
COLEC10 ; TNFRSF11B
0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 1
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9