Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16896398
SLC22A7
6 43294966 upstream gene variant A/T snv 0.42 5
rs11030119
BDNF
11 27706555 intron variant G/A;T snv 3
rs11072518 15 74942269 upstream gene variant T/A;C snv 3
rs7087728
MAT1A
10 80273714 3 prime UTR variant G/A;C snv 3
rs864321650
NKX2-5
5 173234902 missense variant G/A;C snv 3
rs1035543
PKD1L3
16 71949873 missense variant G/C snv 0.39 0.33 2
rs12037987
WNT2B
1 112500200 intron variant T/C snv 8.6E-02 2
rs2073824
ABO
9 133257246 intron variant A/G snv 0.40 2
rs2074633
HDAC9
7 18996297 3 prime UTR variant T/A;C snv 2
rs218966
PHF14
7 10982603 missense variant A/G snv 0.64 0.68 2
rs2285489
ADAMTS13
9 133424254 intron variant T/C snv 0.68 2
rs3851059 10 80270902 downstream gene variant G/A snv 0.27 2
rs3918166
NOS3
7 150996468 missense variant G/A;C snv 3.9E-03; 8.8E-05 2
rs61742245
VKORC1
16 31094624 missense variant C/A;T snv 2.4E-03 2
rs759985000
BDNF
11 27700987 5 prime UTR variant G/A;C snv 4.2E-06; 8.4E-06 2
rs8176668
ABO
9 133268647 intron variant A/T snv 2
rs10089084
IDO1
8 39912430 intron variant G/C snv 0.30 1
rs10123021 9 100689786 regulatory region variant G/A;T snv 1
rs10414398
CEACAM20
19 44517149 missense variant G/A snv 0.14 0.15 1
rs10478723
EDN1
6 12295228 intron variant G/A snv 0.15 1
rs10848683
CACNA1C-AS1 ; CACNA1C
12 2681964 missense variant C/T snv 4.0E-06; 0.78 0.71 1
rs10890917 11 108988857 intergenic variant C/A;G snv 3.5E-02 1
rs11044400 12 19033113 intergenic variant C/T snv 0.13 1
rs11240065
LINC00624
1 147468451 intron variant T/C snv 1
rs112896372 5 3756587 intergenic variant T/C;G snv 1