Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10073892
SLCO6A1
5 102391066 non coding transcript exon variant T/C snv 0.24 0.21 1
rs10512015
ANXA1
9 73166330 intron variant T/C snv 9.9E-02 1
rs16885997 8 114496877 intergenic variant G/T snv 3.5E-02 1
rs17641411
GABRA4
4 46941670 intron variant C/T snv 2.8E-02 1
rs2973488
CTNND2
5 11043805 intron variant A/T snv 0.19 1
rs73643144
TEK
9 27126454 intron variant T/C snv 3.5E-02 1
rs7700443 5 85876294 intergenic variant T/G snv 0.57 1
rs146170087
C19orf12
0.925 0.040 19 29702747 missense variant T/C snv 2.3E-03 1.1E-03 7
rs515726205
C19orf12
0.882 0.040 19 29702966 missense variant C/T snv 2.4E-05 1.4E-05 7
rs7157599
DEGS2
0.925 0.040 14 100159565 missense variant C/T snv 0.73 0.76 6
rs11030108
BDNF ; BDNF-AS
1.000 0.040 11 27673917 intron variant A/G snv 0.72 3
rs1187120 0.925 0.040 6 34182850 intergenic variant T/C snv 0.99 3
rs761715536
ADRA2A
1.000 0.040 10 111079092 stop gained G/A;T snv 6.4E-06; 1.3E-05 3
rs796052957
SCN1A-AS1 ; SCN1A
0.925 0.040 2 166054735 missense variant A/G snv 3
rs1157659 1.000 0.040 11 27736075 intron variant A/G snv 0.37 2
rs115881343
TOMM40
1.000 0.040 19 44899959 intron variant C/G;T snv 2.9E-02 2
rs13333659
CBFA2T3
1.000 0.040 16 88972472 intron variant G/T snv 0.13 2
rs1557372 1.000 0.040 21 41460614 downstream gene variant C/T snv 0.40 2
rs17601241
MIR4713HG ; CYP19A1
1.000 0.040 15 51215677 intron variant G/A snv 0.11 8.6E-02 2
rs2162560
DNMT1
1.000 0.040 19 10168778 intron variant G/A snv 0.35 2
rs2283368
KL
1.000 0.040 13 33019132 intron variant T/C snv 0.15 2
rs457274
MX1
1.000 0.040 21 41420558 5 prime UTR variant C/G snv 0.35 2
rs469083
MX1
1.000 0.040 21 41436789 intron variant C/T snv 0.61 2
rs564919438
MUTYH
1.000 0.040 1 45332421 missense variant G/C;T snv 8.0E-06 2
rs772720363
CHRNA4
1.000 0.040 20 63350819 missense variant C/T snv 4.0E-06 2