Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 1
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 1
rs6740584
CREB1
0.882 0.040 2 207564627 intron variant T/C snv 0.37 1
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 1
rs1488864
LOC101927825 ; CAVIN3
0.851 0.080 11 6321099 intron variant T/G snv 0.80 1
rs1545843
LOC107984536
0.827 0.120 12 84170289 intron variant G/A snv 0.52 1
rs760161369
MTHFR
0.882 0.040 1 11800214 missense variant G/A;C snv 2.8E-05; 4.0E-06 1
rs4512342
NRG1
0.827 0.120 8 32750356 intron variant T/G snv 0.12 1
rs2522833
PCLO
0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 1
rs2984618
TAL1
0.925 0.040 1 47224766 intron variant G/T snv 0.52 1
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 1
rs120074175
TPH2
0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs10233018 0.925 0.040 7 117883655 non coding transcript exon variant A/G snv 0.53 2
rs10485715 0.925 0.040 20 7279278 intergenic variant T/C snv 5.5E-02 2
rs10809520 0.925 0.040 9 11557797 intergenic variant C/T snv 0.28 2
rs4685959 0.925 0.040 3 5645577 regulatory region variant C/G;T snv 2
rs4810896 0.925 0.040 20 48918761 upstream gene variant A/C;G snv 2
rs75921243 0.925 0.040 8 9988356 intron variant T/G snv 1.9E-02 2
rs76767803 0.925 0.040 3 36230378 intergenic variant C/T snv 0.16 2
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 2
rs116609693
ANKRD19P
0.925 0.040 9 92811394 intron variant C/T snv 6.1E-02 2
rs1401635
BDNF ; BDNF-AS
0.925 0.040 11 27672444 intron variant C/G snv 0.73 2
rs1961982
C12orf42
0.925 0.040 12 103218955 intergenic variant G/A snv 0.27 2