Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11157436
TRAV30
0.851 0.040 14 22168978 synonymous variant C/T snv 0.19 7
rs2816992
NR5A2 ; LOC107985244
0.925 0.040 1 200100088 intron variant A/G snv 0.39 4
rs545608
CRYZL2P-SEC16B ; SEC16B
0.925 0.040 1 177929986 intron variant G/C snv 0.20 4
rs10739217
LOC107987108
0.925 0.040 9 105973112 regulatory region variant T/A;C snv 3
rs1392817
PDE4B
0.925 0.040 1 66073773 intron variant A/G snv 0.51 3
rs1828853
MIR4300HG
0.925 0.040 11 82371520 intron variant G/A;C;T snv 3
rs2145839
LOC105372648
0.925 0.040 20 48856501 regulatory region variant G/T snv 0.29 3
rs6871087 0.925 0.040 5 30899410 intergenic variant A/G snv 8.5E-02 3
rs7741741
ADGRG6
0.925 0.040 6 142334664 intron variant T/A;G snv 3
rs10009128 0.925 0.040 4 19511508 intron variant C/T snv 0.34 2
rs10017335
LOC645513
0.925 0.040 4 119460368 intron variant C/G snv 0.28 2
rs10017573
STX18
0.925 0.040 4 4461337 intron variant T/C snv 0.15 2
rs10019193
LOC107986198 ; DDX60L ; PALLD
0.925 0.040 4 168526369 intron variant G/A;C snv 2
rs10059423
CTNND2
0.925 0.040 5 11600827 intron variant A/C;T snv 2
rs10073216 0.925 0.040 5 169390084 intergenic variant A/G snv 5.1E-02 2
rs10086956
PSKH2 ; ATP6V0D2
0.925 0.040 8 86052433 intron variant C/G snv 0.31 2
rs10103696 0.925 0.040 8 90574875 intron variant G/A snv 0.12 2
rs10112240 0.925 0.040 8 31245931 intergenic variant C/T snv 0.19 2
rs10117057 0.925 0.040 9 7577893 intergenic variant G/A snv 2.8E-02 2
rs10119834 0.925 0.040 9 119037865 intergenic variant C/T snv 0.96 2
rs10120294
NDUFA8
0.925 0.040 9 122134810 regulatory region variant A/G snv 0.71 2
rs10122943
GABBR2
0.925 0.040 9 98400981 intron variant C/T snv 6.3E-02 2
rs10136383 0.925 0.040 14 22332649 intron variant C/T snv 6.4E-02 2
rs10141031
NUMB
0.925 0.040 14 73306901 intron variant C/G snv 0.22 2
rs10170968
LOC107985969
0.925 0.040 2 193089825 intergenic variant G/A snv 4.6E-02 2