Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11793831 9 23362313 intron variant G/A;T snv 2
rs118134876
THSD7A
7 11460745 missense variant C/A;T snv 4.0E-02 2
rs12028010 1 41298799 intron variant T/C snv 0.19 2
rs1223397
PHACTR1 ; TBC1D7 ; TBC1D7-LOC100130357
6 13270713 intron variant G/A;C snv 0.19 2
rs12446589
TUFM ; SH2B1
16 28859641 intron variant G/A snv 0.30 2
rs12761761
PPP2R2D
10 131961871 downstream gene variant C/T snv 0.21 2
rs12914495
DENND4A
15 65687454 intron variant A/G;T snv 2
rs13197257
PTPRK
6 128012537 intron variant G/T snv 0.21 2
rs13220261
LOC107986583 ; BTN1A1
6 26498957 upstream gene variant C/A;T snv 2
rs13259607 8 70439812 intergenic variant C/T snv 0.15 2
rs13428598
ARHGAP15
2 143492918 intron variant C/T snv 0.28 2
rs1343775 1 41292321 intron variant A/G snv 0.17 2
rs142601917 12 120914271 upstream gene variant C/A;G;T snv 2
rs143699161
LINC02210-CRHR1 ; LOC105371802
17 45671346 intron variant A/G snv 0.19 2
rs1473634 8 21057805 intron variant A/G snv 0.22 2
rs1492014 3 94352637 intergenic variant T/C;G snv 2
rs1614887
BTN2A2
6 26392793 synonymous variant G/A snv 0.53 0.63 2
rs17043393
ESRRG
1 216698070 intron variant A/G snv 0.13 2
rs17151637
MSRA
8 10295572 intron variant C/G;T snv 2
rs17245822 13 72557556 intergenic variant A/C snv 0.34 2
rs17266097
SATB2
2 199410486 intron variant C/T snv 0.29 2
rs17698580
LOC105370655
14 98080574 intron variant T/C snv 0.21 2
rs1831539
LINC01358
1 59094665 intron variant T/C snv 0.41 2
rs191903670
PFKFB4
3 48540620 intron variant A/T snv 1.1E-02 2
rs1972863
GRID2
4 93658360 intron variant G/A snv 0.40 2