Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs4839421
CYMP
0.925 0.040 1 110479338 intron variant C/A snv 0.40 3
rs11209175
GNG12-AS1
1.000 0.040 1 67909145 intron variant C/T snv 0.54 2
rs116362708
SLC44A5
1.000 0.040 1 75464629 intron variant G/A snv 2.3E-02 2
rs12030991 1.000 0.040 1 106683737 intergenic variant G/C;T snv 2
rs12068879
KAZN
1.000 0.040 1 14959860 intron variant A/G snv 0.18 2
rs12137398
CAMTA1
1.000 0.040 1 7730488 intron variant C/T snv 0.14 2
rs12137936
NEGR1
1.000 0.040 1 72254674 intron variant C/G snv 0.23 2
rs17432675
LMOD1
1.000 0.040 1 201918593 intron variant T/C snv 0.32 2
rs3795310
RERE
1.000 0.040 1 8371547 intron variant C/T snv 0.54 2
rs4554696
PDE4B
1 65942328 intron variant C/T snv 0.33 2
rs6661750
PDE4B
1 66081201 intron variant A/G;T snv 2
rs75507262
LINC02815
1.000 0.040 1 229213737 intergenic variant A/G snv 8.0E-03 2
rs75650221
RABGAP1L
1.000 0.040 1 174452856 intron variant C/T snv 4.1E-02 2
rs913687
RABGAP1L
1.000 0.040 1 174805993 intron variant A/G snv 0.60 2
rs113378111 1.000 0.040 2 9788024 intergenic variant G/A snv 2.8E-02 3
rs34668726
KLHL29
1.000 0.040 2 23673031 intron variant C/G snv 0.13 3
rs35825582
ARHGAP15
1.000 0.040 2 143491193 intron variant G/A snv 0.45 3
rs6546604 0.925 0.040 2 70415675 intron variant G/A;T snv 3
rs78087832 0.925 0.040 2 224600060 intergenic variant C/T snv 2.4E-03 3
rs11693031
ERBB4
1.000 0.040 2 211813206 intron variant A/G;T snv 2
rs13413953
ARHGAP15
1.000 0.040 2 143479467 intron variant T/G snv 0.25 2
rs1375194
LOC105374455
1.000 0.040 2 33601810 intron variant T/C snv 0.42 2
rs16841143
PTH2R
2 208384849 intron variant G/A snv 0.13 2
rs17711053
VWC2L
1.000 0.040 2 214574984 intron variant A/G snv 0.11 2