Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12043259
NFASC
1 204858913 intron variant C/G snv 0.11 2
rs1212415280
VEGFA
6 43771130 missense variant G/T snv 2.1E-05 2
rs17228602
ACHE ; UFSP1
7 100890786 3 prime UTR variant C/T snv 1.5E-02 2
rs2377339
NCK2
2 105840835 intron variant A/G snv 4.8E-02 2
rs1075650
IER5L
9 129176634 3 prime UTR variant T/C snv 0.25 1
rs16918875
OPRK1
8 53229594 synonymous variant G/A snv 4.3E-02 7.1E-02 1
rs1875999
CRHBP
5 76969157 3 prime UTR variant T/C snv 0.38 1
rs2073837
DBH-AS1 ; DBH
9 133657806 intron variant G/A snv 0.31 1
rs382140 7 108141755 intergenic variant A/G snv 0.74 1
rs7118900
ANKK1
11 113396099 missense variant G/A snv 0.25 0.25 1
rs772527880
AGFG1
2 227531108 missense variant G/A snv 4.0E-06 1
rs963549
OPRK1
8 53229264 synonymous variant C/T snv 0.17 0.24 1
rs2251214
SYT1
0.827 0.040 12 79430071 intron variant A/G;T snv 7
rs1040288
NR3C2
1.000 0.040 4 148126966 intron variant G/C snv 0.49 3
rs2180619
CNR1
1.000 0.040 6 88168233 upstream gene variant G/A snv 0.53 3
rs1409568 1.000 0.040 10 118871273 intron variant T/C snv 8.2E-02 2
rs796065354
ESR1
0.882 0.080 6 151944320 missense variant A/G snv 9
rs2070762
TH
0.925 0.080 11 2165105 intron variant A/G snv 0.43 5
rs230530
NFKB1
0.882 0.080 4 102532823 intron variant A/G snv 0.37 4
rs2952621 0.882 0.080 2 129240870 downstream gene variant T/A;C snv 4
rs4436578
DRD2
0.925 0.080 11 113436043 intron variant C/T snv 0.73 4
rs1611131
DBH-AS1 ; DBH
0.925 0.080 9 133657065 splice region variant A/G snv 0.28; 4.0E-06 0.25 3
rs17228616
ACHE ; UFSP1
1.000 0.080 7 100890100 3 prime UTR variant G/T snv 9.8E-02 3
rs604300
MGLL
1.000 0.080 3 127724009 intron variant A/G snv 0.91 3
rs11503014
GABRA2
1.000 0.080 4 46388848 5 prime UTR variant C/G snv 0.27 2