Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs2229616
MC4R
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 22
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
rs1045411
HMGB1
0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 18
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 17
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs1360485
HMGB1
0.742 0.320 13 30457747 3 prime UTR variant C/T snv 0.58 16
rs11727676
HHIP
0.776 0.080 4 144737912 synonymous variant T/C snv 6.6E-02 6.4E-02 14
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 13
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10