Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12071360 1.000 0.080 1 233608833 intergenic variant T/C snv 0.10 1
rs6719226 1.000 0.080 2 25173143 upstream gene variant C/G snv 0.13 1
rs6989250 1.000 0.080 8 53253835 upstream gene variant C/G;T snv 1
rs2229163
CHRM4
1.000 0.080 11 46385307 synonymous variant G/A snv 1.0E-02 3.9E-02 1
rs5374
GALR1
1.000 0.080 18 77250689 synonymous variant T/C snv 0.57 0.57 1
rs6871510
HOMER1
1.000 0.080 5 79496521 intron variant C/T snv 0.22 1
rs6561333
HTR2A
1.000 0.080 13 46846177 intron variant T/C snv 0.60 1
rs1437134
NFAT5
1.000 0.080 16 69696523 3 prime UTR variant A/G snv 0.66 1
rs6713532
POMC
1.000 0.080 2 25161964 intron variant T/C snv 0.36 1
rs111325002 1.000 0.080 3 96134788 intergenic variant A/G snv 8.6E-03 2
rs1868152 0.925 0.080 3 186502274 intergenic variant A/G;T snv 0.85 2
rs779838446
CHRNA6
0.925 0.080 8 42756217 missense variant G/A snv 4.0E-06 7.0E-06 2
rs149775276
CHRNB3
0.925 0.080 8 42732292 missense variant C/T snv 3.6E-04 4.9E-04 2
rs150954431
NCOR2
1.000 0.080 12 124517777 intron variant C/T snv 1.6E-02 2
rs2005290
OR3A2
1.000 0.080 17 3284718 intron variant C/G;T snv 2
rs13273442 0.882 0.080 8 42688874 intergenic variant A/G snv 0.66 4
rs2952621 0.882 0.080 2 129240870 downstream gene variant T/A;C snv 4
rs1042363
AKAP12
0.882 0.080 6 151356693 3 prime UTR variant T/C snv 4
rs2629540
FAM53B
0.925 0.080 10 124737579 intron variant G/C snv 0.18 4
rs10052957
NR3C1
0.851 0.160 5 143407136 non coding transcript exon variant G/A snv 0.28 4
rs1126671
ADH4 ; LOC100507053
0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75 5
rs684513
CHRNA5
0.925 0.080 15 78566058 intron variant C/G;T snv 5
rs6454674
CNR1
0.851 0.120 6 88163211 intron variant T/G snv 0.32 5
rs1079597
DRD2
0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs2234918
OPRD1
0.827 0.200 1 28863085 synonymous variant C/T snv 0.59 0.50 5