Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10500331
RBFOX1
1.000 0.080 16 6114477 intron variant C/T snv 0.15 1
rs10504473
NCOA2
1.000 0.080 8 70348097 intron variant A/C snv 0.24 1
rs10508503 1.000 0.080 10 16257952 intergenic variant C/A;T snv 2
rs1051168
NMB
1.000 0.080 15 84657289 missense variant G/C;T snv 4.5E-06; 0.22 2
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs10521296 1.000 0.080 16 53529332 intergenic variant G/A snv 0.15 1
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs1054135
FABP4 ; LOC101927118
0.851 0.240 8 81478525 3 prime UTR variant C/T snv 0.17 5
rs1057231
LOC100130701 ; FSTL1
1.000 0.080 3 120394556 3 prime UTR variant T/G snv 0.46 1
rs1057515576
ARL6
0.807 0.280 3 97787991 frameshift variant TAT/GAAAA delins 9
rs1057517991
MC4R
0.925 0.120 18 60371539 missense variant A/G snv 4.0E-06 2
rs1057518907
GNAS
0.732 0.320 20 58891811 stop gained C/G;T snv 16
rs1057972
IL15
0.790 0.200 4 141733279 3 prime UTR variant A/T snv 0.54 7
rs1058046
PYY
0.925 0.120 17 43953163 missense variant G/C snv 0.63 0.59 2
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1064891
PFKFB3
0.925 0.080 10 6234611 3 prime UTR variant T/C snv 0.37 2
rs10735104
TRPV4
1.000 0.080 12 109790160 intron variant C/G;T snv 1
rs1075399
TMEM132C
1.000 0.080 12 128463014 intron variant T/G snv 1
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs10783050 1.000 0.080 1 96571527 intergenic variant T/C snv 0.28 1
rs10788528
BMPR1A
1.000 0.080 10 86857014 intron variant G/A snv 0.14 1
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27