Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 14
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 13
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 3
rs12720459
KCNQ1
0.807 0.160 11 2583535 missense variant C/A;G;T snv 3
rs1613662
GP6 ; LOC107985325
0.851 0.120 19 55025227 missense variant G/A snv 0.85 0.83 2
rs1671152
LOC107985325 ; GP6
0.882 0.160 19 55014977 missense variant T/G snv 0.85 0.81 2
rs769825641
CHPT1 ; SYCP3
1.000 0.040 12 101729109 splice region variant A/G snv 5.6E-05 1
rs587776454
GATA1
0.851 0.160 X 48792346 missense variant G/A;C snv 1
rs2236225
MTHFD1
0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 1
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1
rs121918474
PROS1
0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 1
rs9839776
SOX2-OT
0.851 0.160 3 181593779 intron variant C/G;T snv 1