Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4704397
PDE8B
0.807 0.200 5 77222617 intron variant G/A snv 0.54 13
rs1256046734
LEPR
0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 12
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs7830
NOS3 ; ATG9B
0.763 0.320 7 151012483 3 prime UTR variant G/T snv 0.38 0.32 11
rs3918188
NOS3
0.776 0.280 7 151005693 intron variant C/A;T snv 10
rs7069102
SIRT1
0.790 0.440 10 67903362 intron variant C/G snv 0.64 10
rs2273773
SIRT1
0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 9
rs6234
PCSK1 ; LOC101929710
0.851 0.160 5 96393270 missense variant G/C snv 0.27 0.24 8
rs2241423
MAP2K5
0.882 0.120 15 67794500 intron variant G/A snv 0.29 7
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 6
rs2943650 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 6
rs997509
ENPP1
0.827 0.200 6 131846837 intron variant C/T snv 5.3E-02 6
rs1800849
UCP3
0.851 0.160 11 74009120 upstream gene variant G/A;T snv 5
rs6857715
NPY2R ; LOC107986321
0.827 0.160 4 155208030 non coding transcript exon variant C/A;T snv 5
rs8057044
FTO
0.882 0.080 16 53778702 intron variant G/A snv 0.54 5
rs1319501
NAMPT
0.882 0.120 7 106285307 intron variant C/A;T snv 0.76 4
rs2535633
ITIH4 ; ITIH4-AS1
1.000 0.080 3 52825614 intron variant C/G snv 0.48 4
rs743506
NOS3
0.925 0.120 7 151009827 intron variant G/A;C snv 4
rs1996023 0.925 0.120 4 45162620 intergenic variant T/A;G snv 3
rs2016266
SP7
1.000 0.080 12 53334171 intron variant G/A;C snv 3
rs324419
FAAH
0.925 0.120 1 46406314 stop gained T/A;C snv 0.87 3
rs3746619
MC3R
0.925 0.200 20 56248749 5 prime UTR variant C/A snv 0.14 0.21 3
rs3801266
NAMPT
0.925 0.080 7 106283804 intron variant T/C snv 0.26 3
rs406113
GPX6
0.882 0.160 6 28515705 missense variant A/C snv 0.38 0.45 3
rs1010553
STAB1
1.000 0.080 3 52506757 synonymous variant T/C snv 0.53 0.59 2