Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200803778
LINC02010
1.000 0.080 3 146921799 non coding transcript exon variant TTTG/- delins 1.0E-02 1
rs11435035
ARPIN-AP3S2 ; AP3S2 ; MIR5094
1.000 0.080 15 89850718 non coding transcript exon variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTT delins 1
rs113932007 1.000 0.080 11 115620719 intergenic variant TT/-;T;TTT;TTTT;TTTTT delins 1
rs138270994 1.000 0.080 13 22791997 intergenic variant TCTTTG/- delins 2.3E-02 2
rs149935213
SLC30A8 ; LOC105375716
1.000 0.080 8 117158059 intron variant TCT/- delins 2.2E-02 1
rs72156956 1.000 0.080 2 640987 intergenic variant TACA/-;TACATACA delins 1
rs3214606
FLJ13224 ; SINHCAF
1.000 0.080 12 31324008 5 prime UTR variant TAAG/-;TAAGTAAG delins 7.9E-03 1
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 7
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 7
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 3
rs6136
SELP
0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 3
rs6662618 0.882 0.200 1 92469854 downstream gene variant T/G snv 0.75 3
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 3
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 2
rs2908279 1.000 0.080 7 44135258 downstream gene variant T/G snv 0.59 2
rs1063355
HLA-DQB1-AS1 ; HLA-DQB1
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 1
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 1
rs11619726 1.000 0.080 13 36601856 intergenic variant T/G snv 1.2E-02 1
rs138128600 1.000 0.080 13 73190488 upstream gene variant T/G snv 2.5E-04 1
rs163184
KCNQ1
1.000 0.080 11 2825839 intron variant T/G snv 0.40 1
rs2153827 1.000 0.080 10 92664316 downstream gene variant T/G snv 0.33 1
rs244420
NFAT5
1.000 0.080 16 69624093 intron variant T/G snv 0.35 1