Source: ALL
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 98
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 18
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 10
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 10
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 9
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 9
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 7
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs11694173
THADA
0.827 0.080 2 43363760 intron variant G/A snv 0.14 7
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs2287019
QPCTL
1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 7
rs3110697
IGFBP3
0.827 0.160 7 45915430 intron variant A/G snv 0.58 7
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 7
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 7
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7