Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17216707 20 54115823 intergenic variant T/C snv 0.17 6
rs6127099 20 54114863 intergenic variant A/T snv 0.28 5
rs10485165
LOC105377885
6 88403098 intron variant C/G;T snv 3
rs2302190
MTMR4
17 58507147 missense variant T/A;C snv 0.24 3
rs78862524
ADAMTS3
4 72305473 intron variant C/A snv 3.9E-02 3
rs1007392
PDE3B
11 14753045 intron variant A/G snv 0.35 2
rs10745742
AMDHD1
12 95964751 intron variant C/T snv 0.48 2
rs11023332
PDE3B
11 14762564 intron variant G/C snv 0.35 2
rs11586313 1 152917994 TF binding site variant G/A;C snv 0.51 2
rs116970203
PDE3B
11 14855172 intron variant G/A snv 2.2E-02 2
rs117300835 11 15097429 intergenic variant G/A snv 7.6E-03 2
rs117865811
SPON1
11 14180763 intron variant A/G snv 6.3E-03 2
rs117913124
CYP2R1
11 14879385 synonymous variant G/A snv 1.7E-02 1.6E-02 2
rs12287212 11 14428315 intergenic variant C/A snv 0.31 2
rs12868495 13 34067425 intergenic variant G/A snv 2.3E-02 2
rs13107347
NPFFR2
4 72109031 intron variant T/C snv 0.32 2
rs138485827 4 72166226 intergenic variant C/T snv 5.0E-02 2
rs1410656 13 46968386 intergenic variant T/C snv 0.97 2
rs148189294 4 71575200 downstream gene variant G/A snv 2.6E-02 2
rs1526692 4 71713007 intergenic variant A/G snv 0.41 2
rs156299
LOC107986777
7 24185113 intergenic variant T/G snv 0.53 2
rs1607741 4 71853316 intergenic variant G/C snv 0.65 2
rs17767445 4 71879550 intergenic variant G/A snv 0.20 2
rs182244780
RRAS2
11 14363985 intron variant G/A snv 6.0E-03 2
rs185378533
FLJ42102
11 71422087 intron variant A/G snv 0.68 2