Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8179
CDK6
0.882 0.080 7 92606850 3 prime UTR variant T/A;C;G snv 8
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48 7
rs13117307
EXOC1
0.827 0.080 4 55885574 intron variant C/T snv 0.21 6
rs2566
LAMB3
0.882 0.080 1 209615169 3 prime UTR variant G/A snv 0.27 6
rs7213430
BRIP1
0.851 0.080 17 61682813 3 prime UTR variant G/A snv 0.61 6
rs10802996
EXO1
0.882 0.080 1 241847325 upstream gene variant C/A;G snv 5
rs10893506
ST3GAL4
0.882 0.080 11 126406065 5 prime UTR variant T/A;C snv 6.4E-06; 0.41 5
rs11568785
TGFBR1
0.882 0.080 9 99143552 intron variant A/G;T snv 7.2E-02 5
rs42033
CDK6
0.882 0.080 7 92608219 3 prime UTR variant A/T snv 0.16 5
rs1007541
FSHR
0.882 0.080 2 48981895 intron variant C/T snv 0.16 4
rs1474348
IL6-AS1 ; IL6
0.882 0.080 7 22728289 intron variant C/G snv 0.71 4
rs16970849
TMC8
0.882 0.080 17 78137827 intron variant G/A;T snv 0.11; 4.0E-06 4
rs2289937
RAD21
0.882 0.080 8 116861572 intron variant G/A;C snv 4
rs2290907
TNRC6C
0.882 0.080 17 78097596 intron variant T/C snv 0.23 4
rs4570
UTP23 ; RAD21
0.882 0.080 8 116846150 3 prime UTR variant G/A snv 0.70 4
rs4579555
RAD21
0.882 0.080 8 116867092 intron variant A/G snv 4
rs673
TNF
0.882 0.080 6 31575318 upstream gene variant G/A snv 1.8E-02 4
rs746700511
PDXP
0.851 0.080 22 37665657 missense variant T/C snv 4.0E-06 4
rs750553272
NFE2L2
0.851 0.080 2 177230898 missense variant G/A snv 1.2E-05 7.0E-06 4
rs9277952 0.851 0.080 6 33236497 upstream gene variant G/A snv 0.10 4
rs1003897973
LOC107985302 ; TRIP10
0.882 0.080 19 6746039 missense variant C/G snv 3
rs1030389
SNHG14 ; PWAR6
0.882 0.080 15 25032641 non coding transcript exon variant A/G snv 0.41 3
rs10426502
MYDGF ; TNFAIP8L1
0.882 0.080 19 4651257 intron variant G/A snv 6.8E-02 3
rs1045935
PWAR6 ; SNHG14
0.882 0.080 15 25036439 non coding transcript exon variant G/A;T snv 3
rs1048512
PIGM ; KCNJ10
0.882 0.080 1 160025108 3 prime UTR variant G/A;T snv 0.13 3