Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs2145272 20 6645571 intergenic variant G/A;T snv 7
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 5
rs10842707 12 26318431 intron variant C/G;T snv 4
rs1443512 12 53948900 downstream gene variant A/C;T snv 4
rs17819328 3 12447843 intergenic variant T/A;G snv 4
rs2033529
TDRG1
6 40380914 intron variant A/C;G snv 4
rs2820436
LYPLAL1-AS1
0.882 0.040 1 219467338 intergenic variant A/C;G snv 4
rs7162542
ADAMTSL3
15 83845538 intron variant C/A;G;T snv 4
rs9435732
MFAP2
1 16981663 intron variant C/G;T snv 4
rs11897119
MEIS1
2 66544868 intron variant T/A;C snv 3
rs2764261
FOXO3
6 108606639 intron variant A/G;T snv 3
rs3936510
C5orf67
1.000 0.040 5 56565039 intron variant G/A;T snv 3
rs4765219
CCDC92
12 123955563 intron variant C/A;T snv 3
rs6090583
EYA2
20 46930192 intron variant A/C;G snv 3
rs7164727 15 72801650 downstream gene variant C/G;T snv 3
rs754133
HOXC6 ; HOXC4 ; HOXC5
12 54025136 intron variant G/A;C snv 3
rs757318
CRTC1
19 18709498 intron variant C/A;G;T snv 3
rs757608 17 61419916 regulatory region variant A/G;T snv 3
rs7715806 5 75738562 intergenic variant C/G;T snv 3