Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs737267
SLC2A9
0.851 0.240 4 9933120 intron variant G/A;T snv 4
rs2622621
ABCG2
0.851 0.240 4 88109768 intron variant C/A;G snv 3
rs733175
SLC2A9
0.851 0.240 4 10048517 intron variant C/T snv 0.77 3
rs13198474
SLC17A3
0.851 0.240 6 25874195 5 prime UTR variant G/A snv 4.0E-02 2
rs2079742
BCAS3
0.851 0.240 17 61388336 non coding transcript exon variant T/C snv 0.20 2
rs2941471
HNF4G
0.851 0.240 8 75558169 intron variant G/A snv 0.65 2
rs4766566
CUX2
0.851 0.200 12 111269073 intron variant C/T snv 0.42 2
rs4971059
TRIM46
0.851 0.200 1 155176305 intron variant G/A snv 0.34 2
rs8032477
IGF1R
0.851 0.200 15 98711325 intron variant C/A;T snv 2
rs853679
ZSCAN31
0.851 0.160 6 28329086 intron variant C/A snv 0.20 2
rs9426886
TRIM46
0.851 0.200 1 155179278 intron variant A/T snv 0.40 2
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 6
rs1919128
C2orf16
0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 6
rs3749147
GPN1 ; CCDC121
0.882 0.120 2 27629051 missense variant G/A snv 0.23 0.20 6
rs7756117
H3C3
0.882 0.160 6 26046337 upstream gene variant G/A snv 0.69 5
rs9472138
LOC107986598
0.882 0.160 6 43844025 downstream gene variant C/T snv 0.24 5
rs1165196
SLC17A1
0.882 0.200 6 25812922 missense variant G/A snv 0.62 0.66 4
rs1165215
SLC17A1
0.882 0.200 6 25798704 3 prime UTR variant G/A snv 0.66 4
rs12056034
BAZ1B
0.882 0.160 7 73464315 intron variant A/G snv 9.2E-02 4
rs13197601
SLC17A1
0.882 0.200 6 25785707 intron variant G/A snv 0.32 4
rs199750 0.882 0.160 6 26016234 upstream gene variant C/T snv 0.77 4
rs2230655
H2AC4 ; H3C2
0.882 0.160 6 26033278 synonymous variant G/A snv 0.71 0.76 4
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 4
rs2762353
SLC17A1
0.882 0.200 6 25794203 intron variant A/G snv 0.66 4