Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 29
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 15
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 14
rs11727676
HHIP
0.776 0.080 4 144737912 synonymous variant T/C snv 6.6E-02 6.4E-02 14
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 12
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 10
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 10
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 9
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8