Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs798502
AMZ1 ; GNA12
1.000 0.040 7 2750246 intron variant A/C;G snv 4
rs10010325
TET2 ; TET2-AS1
1.000 0.040 4 105185196 intron variant C/A;G;T snv 3
rs11064881
CIT
1.000 0.040 12 119709120 intron variant G/A snv 5.0E-02 3
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 3
rs2189234
TET2
1.000 0.040 4 105154341 intron variant T/G snv 0.62 3
rs6667605
LOC100996583
1.000 0.040 1 2571341 downstream gene variant C/T snv 0.53 3
rs1077773
KCCAT333
1.000 0.040 7 17403055 intron variant G/A;C snv 2
rs10797432
LOC100996583
1.000 0.040 1 2569899 downstream gene variant C/T snv 0.51 2
rs111456533
EEF1AKMT2
1.000 0.040 10 124750812 intron variant G/A snv 0.18 2
rs11150589
ITGAL
1.000 0.040 16 30471173 upstream gene variant T/A;C;G snv 2
rs11548656
PLCG2
1.000 0.040 16 81883307 missense variant A/G snv 2.5E-02 2.7E-02 2
rs11554257 1.000 0.040 9 114842790 upstream gene variant T/C snv 0.13 2
rs11672983 1.000 0.040 19 54871595 upstream gene variant G/A snv 0.35 2
rs16940202 1.000 0.040 16 85980635 intron variant T/C snv 0.15 2
rs17229285
LOC105373831
1.000 0.040 2 198658398 intron variant C/A;T snv 2
rs17656349
CAMK2A
1.000 0.040 5 150226431 intron variant C/T snv 0.45 2
rs1811711
CCL20
1.000 0.040 2 227805760 5 prime UTR variant C/A;G snv 2
rs2395128
DUPD1
1.000 0.040 10 75052692 intron variant G/T snv 0.32 2
rs254560
C5orf66
1.000 0.040 5 135107916 intron variant G/A snv 0.32 2
rs2651244 1.000 0.040 1 70529879 upstream gene variant G/A snv 0.30 2
rs2858829 1.000 0.040 6 116447754 intron variant A/G snv 0.33 2
rs35675666
PARK7
1.000 0.040 1 7961913 5 prime UTR variant G/C;T snv 2
rs4380874 1.000 0.040 7 107839870 intergenic variant T/A;C;G snv 2
rs4676408 1.000 0.040 2 240634984 downstream gene variant G/A;T snv 0.57 2
rs4743820
LINC00484 ; LOC100507103
1.000 0.040 9 91166134 non coding transcript exon variant C/T snv 0.61 2