Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2414476
TEX9
1.000 0.040 15 56409302 intron variant C/A snv 1.00 1
rs2139240
SLC2A9
0.925 0.120 4 9796468 intron variant T/C snv 1.00 2
rs7698775 0.925 0.120 4 9627427 intron variant T/C snv 1.00 2
rs2325562
KLF12
1.000 0.080 13 73772955 intron variant G/T snv 1.00 1
rs6765789
TGM4
3 44897094 intron variant A/C snv 1.00 1
rs3211852
CD36
7 80654305 intron variant A/G snv 0.99 2
rs6838199 0.925 0.120 4 9619709 intron variant G/C snv 0.99 2
rs10897203 11 62011041 downstream gene variant A/C snv 0.99 1
rs799882
LINC00536
8 116248203 intron variant G/A snv 0.99 2
rs3745442
LAIR1
19 54361091 missense variant G/C snv 0.99 1
rs1857728 1.000 0.080 12 60331608 intergenic variant T/G snv 0.99 1
rs9971916
PDE3A
12 20535707 intron variant A/T snv 0.99 2
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs7836010
EXT1
8 117849128 intron variant G/C snv 0.99 1
rs7955371
WNK1
12 885321 missense variant G/C snv 1.00 0.99 1
rs830948
LRP2
2 169358254 intron variant G/A snv 0.99 3
rs928382 1.000 0.080 10 120122169 regulatory region variant C/G snv 0.99 1
rs2973662
TENM2
5 167783467 intron variant A/G snv 0.98 1
rs556766
PIGO
9 35089051 3 prime UTR variant A/C snv 1.00 0.98 1
rs6460606 1.000 0.080 7 70969613 intergenic variant C/G snv 0.98 1
rs2227246
NME7
1 169238941 intron variant C/T snv 0.98 1
rs1894692 1 169498416 non coding transcript exon variant G/A snv 0.98 2
rs1912439
NOS1AP
1 162324355 intron variant A/G snv 0.98 2
rs1925335 1.000 0.080 1 196211214 intergenic variant A/G snv 0.98 1
rs2465625 12 46956964 regulatory region variant G/T snv 0.98 1