Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 25
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 19
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 19
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 11
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 7
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41 7
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 6
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 5
rs4410790
LOC101927609 ; AHR
0.882 0.160 7 17244953 intron variant T/C snv 0.54 5
rs864745
JAZF1
0.763 0.320 7 28140937 intron variant T/C snv 0.41 5
rs3784099
RAD51B
0.807 0.320 14 68283210 intron variant G/A snv 0.43 4
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 4
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 4
rs6020712
CTNNBL1
1.000 0.080 20 37758210 intron variant G/A snv 0.12 4
rs6763931
ZBTB38
0.925 0.080 3 141383991 intron variant G/A snv 0.54 4
rs721048
EHBP1
0.851 0.200 2 62904596 intron variant G/A snv 0.13 4
rs10934853
EEFSEC
0.882 0.160 3 128319530 intron variant C/A snv 0.43 3
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs12500426
PDLIM5
0.851 0.240 4 94593458 intron variant A/C snv 0.54 3
rs12621278
ITGA6
0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 3
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 3
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 3