Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16913693
ELP1
9 108918079 intron variant T/G snv 8.4E-02 2
rs1483121 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 3
rs11782386 8 9344277 intron variant C/T snv 9.7E-02 2
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs3778321
RREB1
6 7250037 3 prime UTR variant G/A snv 0.11 2
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 3
rs11603334
ARAP1
1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 4
rs6072275
TOP1 ; PLCG1-AS1
20 41115265 intron variant G/A snv 0.13 2
rs17265513
ZHX3
0.925 0.160 20 41203988 missense variant T/C snv 0.14 0.14 2
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs2305929
RBKS ; MRPL33 ; BABAM2-AS1 ; BABAM2
1.000 0.040 2 27891044 intron variant A/G snv 0.14 3
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 2
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 5
rs5394
SLC2A2
3 171027104 intron variant G/A snv 0.15 2
rs3783347
WARS1
14 100372924 intron variant G/T snv 0.16 2
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 4
rs2300615
GLP1R
6 39071727 intron variant T/G snv 0.17 2
rs11672660
GIPR ; MIR642B
19 45676926 intron variant C/T snv 0.18 0.17 2
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 3
rs2268575
GCK ; LOC105375258
7 44149675 intron variant T/C snv 0.18 2
rs4775471 15 62132450 intergenic variant C/T snv 0.18 2
rs11039182
MADD
11 47325172 intron variant T/C snv 0.19 2
rs7944584
MADD
1.000 0.080 11 47314769 intron variant A/T snv 0.19 3
rs11717195
ADCY5
1.000 0.080 3 123363551 intron variant T/C snv 0.19 3
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4