Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9524885
ABCC4
13 95283335 intron variant T/C snv 0.63 2
rs943552 1 156885826 downstream gene variant C/T snv 9.7E-02 2
rs941601
SERPINA6
14 94305204 intron variant C/T snv 0.19 1
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs8904
NFKBIA
0.925 0.120 14 35402011 3 prime UTR variant G/A;C;T snv 0.39; 4.0E-06 4
rs887200
ARVCF
22 19976143 intron variant C/T snv 0.74 1
rs885479
MC1R
0.732 0.280 16 89919746 missense variant G/A snv 0.15 8.3E-02 16
rs879254102
SCN9A ; SCN1A-AS1
2 166277257 missense variant C/T snv 1
rs8136867
MAPK1
0.882 0.080 22 21850504 intron variant G/A snv 0.55 4
rs806378
CNR1
1.000 0.040 6 88149832 intron variant C/T snv 0.21 2
rs80338958
SCN4A
0.790 0.200 17 63945614 missense variant C/A;T snv 1.6E-05; 5.6E-05 9
rs80338761
SEPTIN9
0.882 0.080 17 77402298 missense variant C/T snv 4
rs8007267 0.882 0.200 14 54912273 intergenic variant C/T snv 0.31 6
rs80026734
CYP3A5 ; ZSCAN25
7 99676132 missense variant C/T snv 1
rs796590326
P2RX7 ; LOC105370032
0.851 0.200 12 121162449 missense variant GT/AC mnv 5
rs7958311
P2RX7 ; LOC105370032
0.851 0.160 12 121167552 missense variant G/A;C snv 0.25; 4.0E-06 5
rs7824175
OPRK1
8 53231614 intron variant C/G;T snv 1
rs781565158
PYROXD1
0.851 0.120 12 21452130 missense variant A/G snv 4.7E-05 2.1E-05 22
rs778056858
NTRK1
1.000 0.080 1 156866944 missense variant T/C snv 8.0E-06 7.0E-06 2
rs7734804
LOC105377703
5 164919530 intron variant G/T snv 8.3E-02 2
rs773030005
UGT2B7
1.000 0.040 4 69107204 synonymous variant A/C;G snv 4.0E-06; 6.8E-05 2
rs7718461
CRHBP
5 76962223 intron variant A/G snv 0.51 1
rs77114424
OPRM1
6 154039497 missense variant G/A snv 2
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36