Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35738585 1.000 0.040 11 113515625 intergenic variant T/G snv 0.40 2
rs12420205 1.000 0.040 11 113523313 intergenic variant C/T snv 0.65 2
rs7937477 1.000 0.040 11 113545374 intergenic variant A/T snv 0.59 2
rs7927693 1.000 0.040 11 113554746 intergenic variant G/A snv 0.57 2
rs4373974 1.000 0.040 11 113559764 intergenic variant T/G snv 0.40 2
rs61687445 1.000 0.040 11 113567370 intergenic variant C/A snv 0.35 2
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs190662943
DPP10
1.000 0.040 2 115195009 intron variant G/A snv 5.6E-04 2
rs59382200
LOC105374054
1.000 0.040 3 117240427 intergenic variant A/G snv 0.29 2
rs41279104
NOS1
0.827 0.160 12 117439680 intron variant C/T snv 0.11 6
rs13296664 1.000 0.040 9 117684418 downstream gene variant C/T snv 0.22 2
rs2149351 1.000 0.040 9 117739366 intron variant T/G snv 0.81 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs60393230
LOC107987122
1.000 0.040 9 119893005 intergenic variant A/G;T snv 2
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs1994321 1.000 0.040 11 12065766 upstream gene variant G/T snv 0.33 3
rs7714426
PRR16
1.000 0.040 5 120683373 intron variant C/A;G;T snv 2
rs208294
P2RX7 ; LOC105370032
0.790 0.320 12 121162450 missense variant T/A;C;G snv 0.51 9
rs2230912
P2RX7 ; LOC105370032
0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs1653625
LOC105370032 ; P2RX7
12 121185082 3 prime UTR variant C/A;G snv 1
rs57506017 1.000 0.040 7 12205599 intergenic variant A/T snv 0.28 2
rs77087420
KIAA1109
1.000 0.040 4 122201701 intron variant A/G snv 3.4E-02 2
rs10950393
TMEM106B
1.000 0.040 7 12223920 intron variant T/C snv 0.50 2