Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 5
rs5762862
ZNRF3
22 28856744 intergenic variant G/A;T snv 4
rs34887403
HSCB
22 28755162 intron variant G/A snv 0.11 2
rs7286472 22 33990484 intergenic variant A/G snv 0.19 2
rs139055942
TNRC6B
22 40318352 intron variant C/G snv 4.1E-02 1
rs8139817
MICAL3
22 17985603 intron variant A/C snv 0.34 1
rs9609429
AP1B1P1 ; LOC105373000
22 32121444 upstream gene variant T/C snv 0.25 1
rs9306160
RRP1B
0.925 0.080 21 43687681 missense variant T/C snv 0.69 0.73 5
rs112204826 21 43301147 TF binding site variant C/T snv 2.9E-02 2
rs117870289
ERG
21 38611524 intron variant C/T snv 7.7E-03 2
rs12627651 21 43340723 intergenic variant G/A snv 0.22 2
rs62229372
MORC3
21 36320209 5 prime UTR variant C/T snv 0.11 2
rs35123175
HSF2BP
21 43586730 intron variant A/- delins 6.0E-02 1
rs79094191 21 43301010 regulatory region variant T/C snv 3.7E-02 1
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs867186
PROCR ; MMP24-AS1-EDEM2
0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 15
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 7
rs6021247
NFATC2
1.000 0.080 20 51492442 intron variant G/A snv 0.65 7
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs6108787 20 10986566 intron variant T/G snv 0.46 5
rs1407040
GNAS
20 58897119 intron variant C/T snv 0.70 4
rs6031431
JPH2
20 44166512 intron variant A/G snv 0.46 4
rs6026740
ZNF831
20 59165293 intron variant A/G snv 0.15 3