Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1883415
GPLD1
0.925 0.040 6 24491247 intron variant A/C snv 0.34 1
rs7923609
MIR1296 ; JMJD1C
10 63374062 intron variant A/G snv 0.43 1
rs1976403
NBPF3
1 21439960 upstream gene variant A/C snv 0.33 1
rs11216930
PHLDB1
1.000 0.040 11 118618067 intron variant A/C snv 0.22 1
rs2236653
ST3GAL4
11 126413890 intron variant C/T snv 0.45 1