Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2142672 6 16196963 intergenic variant G/A snv 0.42 2
rs2346102 1 163888348 intergenic variant G/T snv 2.4E-02 2
rs2927453 19 44767927 downstream gene variant C/A;T snv 2
rs4560142 2 21160845 intergenic variant C/T snv 0.75 2
rs488507 2 21170817 intergenic variant G/T snv 0.78 2
rs538928 2 21166147 intergenic variant A/G;T snv 2
rs576203 2 21170751 intergenic variant A/G snv 0.76 2
rs17110922
ABCA4
1 94043489 intron variant A/T snv 2.5E-03 9.9E-03 2
rs9590177
ABCC4
13 95083956 intron variant C/T snv 3.4E-02 2
rs1146586
ACADM
1 75762289 intron variant C/A;T snv 2
rs11854545
ACAN
15 88825873 intron variant G/A;T snv 2
rs28730839
ACE
17 63483140 missense variant C/A;G snv 4.0E-06; 4.8E-04 2
rs34043481
ADCY2
5 7520816 missense variant G/A snv 5.1E-04 2.2E-03 2
rs1826361
AGTR1
3 148726941 intron variant A/C snv 0.13 2
rs267733
ANXA9
1 150986360 missense variant A/G snv 0.12 0.12 2
rs8178926
APOH
17 66220473 intron variant C/T snv 1.7E-02 2
rs8178944
APOH
17 66213260 intron variant C/T snv 1.4E-02 2
rs1407717
ATP1A1
1 116370991 upstream gene variant T/C snv 2.3E-02 2
rs2229459
BDKRB1
14 96264431 missense variant C/T snv 2.9E-04 3.9E-04 2
rs4942486
BRCA2
13 32379251 intron variant T/C snv 0.52 2
rs6697608
C8A
1 56897364 intron variant G/A snv 2.6E-02 2
rs6697767
C8A
1 56860400 intron variant A/G snv 2.5E-02 2
rs7339932
C8A
1 56867810 intron variant G/T snv 3.8E-02 2
rs4647641
CASP3
4 184640236 intron variant T/G snv 3.6E-02 2
rs4647600
CASP3 ; PRIMPOL
4 184649745 5 prime UTR variant T/C;G snv 2