Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs142320277
LRP1B
1.000 0.080 2 140665410 intron variant G/A;C snv 2
rs149317277
ITGB8
0.925 0.080 7 20384300 intron variant -/GAAACAAGATTCT;GAACCAAGATTCT delins 0.36 2
rs149647891
PDE7B
1.000 0.080 6 136006932 intron variant C/T snv 1.5E-02 2
rs1612986 0.925 0.080 10 9022753 intergenic variant T/C snv 0.24 2
rs1617333
CD247
0.925 0.080 1 167467033 intron variant A/G snv 0.27 2
rs1696361 0.925 0.080 12 120926020 TF binding site variant T/C snv 0.75 2
rs17103286 0.925 0.080 14 35415835 regulatory region variant A/C;G snv 2
rs1806656
ILDR1
0.925 0.080 3 121997324 intron variant C/G snv 0.23 2
rs1861245
IL18R1 ; IL1RL1
0.925 0.080 2 102350446 intron variant C/T snv 2
rs188074962 0.925 0.080 12 120927628 intergenic variant G/A snv 0.79 2
rs1885013
RAD51B
0.925 0.080 14 68287978 intron variant G/A snv 0.57 2
rs1887704
UBAC2
0.925 0.080 13 99322238 intron variant C/G snv 0.55 2
rs1893380 0.925 0.080 18 51121270 intergenic variant G/A;C;T snv 2
rs201541519 1.000 0.080 14 105694756 intergenic variant AAGA/- delins 1.2E-02 2
rs2052690
MRVI1
0.925 0.080 11 10642486 intron variant G/T snv 0.22 2
rs2221641 0.925 0.080 8 80382467 intron variant C/T snv 0.51 2
rs2299012
RAD50
0.925 0.080 5 132581248 intron variant A/C;T snv 2
rs2450083
COLEC10
1.000 0.080 8 119051303 intron variant T/C snv 0.59 2
rs274943
LOC101929563
0.925 0.080 9 23585841 intron variant T/C snv 0.48 2
rs2766667
LOC101927770
0.925 0.080 20 53555865 intron variant T/C;G snv 2
rs28407950
HLA-DQB1-AS1
0.925 0.080 6 32658571 upstream gene variant C/T snv 0.29 2
rs28522747 0.925 0.080 6 35166952 regulatory region variant G/A snv 0.22 2
rs2918302
LINC01862 ; LOC107983991
0.925 0.080 19 8675909 intron variant G/A snv 0.19 2
rs3116989
LOC105375021 ; HLA-DPA3
0.925 0.080 6 33131761 intron variant G/T snv 0.16 2
rs340934 0.925 0.080 9 6081804 intergenic variant G/C;T snv 2