Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12509976
MTTP
4 99596167 intron variant C/T snv 7.7E-02 1
rs13132430 4 99302913 downstream gene variant G/A;C snv 1
rs2602836
LOC100507053
4 99093654 intron variant A/G snv 0.50 1
rs34311866
TMEM175
0.882 0.080 4 958159 missense variant T/C snv 0.18 0.14 4
rs10874777 1 93396463 intergenic variant T/A;C snv 1
rs4847240
DR1
1 93352389 intron variant A/G snv 0.51 3
rs12133576
DR1
1.000 0.040 1 93350843 intron variant A/G snv 0.51 3
rs1461729
LOC157273
1.000 8 9329732 intron variant A/G snv 0.88 3
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 4
rs6601299
LOC157273
0.925 0.040 8 9327181 intron variant T/C snv 0.88 3
rs4240624
LOC157273
0.882 0.040 8 9326721 intron variant G/A snv 0.87 2
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87 6
rs6685271
TMED5
1 93169033 intron variant C/A snv 0.61 1
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 5
rs7895716
EXOC6
10 93024020 intron variant C/G snv 0.32 1
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs290986
SYK
1.000 0.080 9 90801254 upstream gene variant A/G snv 0.18 2
rs139271800
PLIN1
15 89671546 missense variant A/G snv 3.1E-04 4.0E-04 1
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs4883201
PHC1
12 8929985 intron variant A/G snv 8.6E-02 3
rs3822072
FAM13A
4 88820118 intron variant G/A;C snv 2
rs13133548
FAM13A
4 88818977 intron variant G/A snv 0.49 1