Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1108143 1.000 0.080 2 234557214 regulatory region variant A/G snv 8.1E-02 1
rs17042407 1.000 0.080 2 112801337 intergenic variant T/C snv 0.23 1
rs7624041 1.000 0.080 3 94389819 intergenic variant G/A snv 0.89 1
rs7849280
ABO
1.000 0.080 9 133251249 non coding transcript exon variant A/G snv 1
rs372481703
APC
1.000 0.080 5 112839106 missense variant G/A snv 1.6E-05 1.4E-05 1
rs80142782
ASH1L
1.000 0.080 1 155515236 intron variant T/C snv 2.9E-03 1
rs7712641
LINC02161
1.000 0.080 5 89607147 intron variant T/A;C snv 1
rs10029005
LINC02516
1.000 0.080 4 124530209 intron variant G/A snv 0.40 1
rs1635566
PADI4
1.000 0.080 1 17356662 intron variant A/G snv 0.70 1
rs882537
PADI4
1.000 0.080 1 17333552 intron variant A/G snv 0.64 1
rs10509671
PLCE1
1.000 0.080 10 94309297 intron variant T/G snv 0.24 1
rs6897169
PTGER4 ; TTC33
1.000 0.080 5 40726036 intron variant C/A;T snv 0.24 1
rs367807476
STK11
1.000 0.080 19 1223035 missense variant C/G;T snv 9.2E-06 1.4E-05 1
rs202208566
TCHP
1.000 0.080 12 109903156 missense variant T/C snv 6.5E-04 1.7E-04 1
rs1203145163
TFF1 ; LOC105372815
1.000 0.080 21 42363329 missense variant C/A snv 7.0E-06 1
rs11040869 0.925 0.080 11 1263382 downstream gene variant G/A snv 1.8E-02 2
rs11088680 0.925 0.080 21 13514758 upstream gene variant A/G snv 0.30 2
rs1887427 0.925 0.080 9 4979730 upstream gene variant A/G snv 0.21 2
rs1892901 0.925 0.080 11 65903422 upstream gene variant G/A snv 9.5E-03 2
rs26160 0.925 0.080 5 145353893 intron variant T/C snv 4.5E-03 2
rs36012910 0.925 0.080 2 25345310 upstream gene variant A/C;G snv 2
rs4145643 0.925 0.080 10 60803097 regulatory region variant G/C;T snv 2
rs283411
ADH1C ; ADH1B
0.925 0.080 4 99344800 intron variant C/A;T snv 2
rs16941667
ALDH2
0.925 0.080 12 111806609 intron variant C/T snv 8.6E-02 2
rs1279599
AMD1
0.925 0.080 6 110879025 intron variant G/A snv 0.87 2