Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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 6
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
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
rs60393230
LOC107987122
1.000 0.040 9 119893005 intergenic variant A/G;T snv 2
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
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
rs201921722 0.925 0.040 11 123679999 downstream gene variant -/A delins 9.2E-06 3
rs73720034 1.000 0.040 7 125794995 intergenic variant T/C snv 7.2E-02 3
rs11605020
LOC105369562
1.000 0.040 11 127110970 intron variant G/A;C snv 2
rs2402960
LOC105375501
1.000 0.040 7 129765934 intron variant C/T snv 0.71 2
rs73788091
FSTL4 ; MIR1289-2
1.000 0.040 5 133429517 intron variant C/T snv 0.10 3
rs6795372 1.000 0.040 3 136765048 intergenic variant T/G snv 0.42 2
rs201569130 0.925 0.040 6 1402916 intergenic variant GACA/- delins 1.1E-02 3
rs142484554
SPSB4
0.925 0.040 3 141059454 intron variant GAG/- delins 0.11 3
rs190783615 0.925 0.040 X 142772620 intergenic variant T/C snv 9.3E-03 3
rs13413953
ARHGAP15
1.000 0.040 2 143479467 intron variant T/G snv 0.25 2