Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2247607
AZGP1
7 99977115 intron variant T/A;C snv 1
rs1119257
CNTN5
11 99791193 intron variant G/A snv 0.27 1
rs17782474
AFF3
2 99649474 intron variant A/G snv 6.6E-02 1
rs6715321 1.000 0.040 2 99492539 upstream gene variant C/A;T snv 0.41 1
rs6761390
REV1
2 99490335 upstream gene variant C/A;G;T snv 1
rs3792142
REV1
2 99440746 intron variant C/A;T snv 1
rs7048860 9 99378849 upstream gene variant A/T snv 0.17 1
rs10819655 9 99352018 downstream gene variant A/T snv 0.37 1
rs10988775 9 99346694 regulatory region variant T/C snv 0.16 1
rs17576589
CNTN5
11 99270087 intron variant C/T snv 0.28 1
rs2748809
BCL11B
14 99268896 intron variant T/C snv 0.30 1
rs1405238
BCL11B
14 99267617 intron variant C/T snv 0.69 1
rs10893002
CNTN5
11 99256521 intron variant T/A snv 0.32 1
rs987773 6 99154010 intergenic variant C/G;T snv 1
rs62323189
EIF4E
4 98874312 3 prime UTR variant T/C snv 0.26 1
rs3823036
POU3F2
6 98836656 3 prime UTR variant T/C snv 0.31 2
rs12060706 1 98791206 intergenic variant C/T snv 0.30 1
rs56242843
SNX7
1 98723043 intron variant C/T snv 0.27 1
rs10783100
SNX7
1 98710740 intron variant T/G snv 0.51 1
rs62491302 8 9852941 intergenic variant G/A snv 9.8E-02 1
rs3783007
STK24
13 98457562 intron variant T/C;G snv 1
rs9556958
FARP1 ; STK24
1.000 0.040 13 98447792 3 prime UTR variant C/G;T snv 3
rs9513414
FARP1
13 98400467 3 prime UTR variant C/G snv 0.12 1
rs9375403 6 98383760 intron variant G/C snv 0.18 1
rs221013
PAK5
20 9834880 intron variant T/A;C snv 1