Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7005834
CCN4
0.827 0.160 8 133201961 intron variant C/A;T snv 6
rs2069812
IL5
0.851 0.240 5 132544224 intron variant A/G snv 0.54 5
rs11675434
TPO
0.827 0.240 2 1404043 non coding transcript exon variant C/T snv 0.39 5
rs179247
TSHR
0.882 0.160 14 80966202 intron variant A/G snv 0.40 5
rs3753793
CCN1 ; DDAH1
0.851 0.240 1 85580205 upstream gene variant A/C snv 0.26 4
rs13143866
IL21 ; IL21-AS1
0.851 0.200 4 122619603 intron variant G/A snv 0.24 4
rs1061501
IRF7
0.851 0.200 11 614864 synonymous variant C/T snv 0.83 0.85 4
rs11611206
LOC105369818 ; MDM1
0.851 0.200 12 68274666 intron variant G/A snv 0.15 4
rs11250144
BLK
0.925 0.200 8 11528767 intron variant G/A;C snv 2
rs2267873
DIO2
0.925 0.160 14 80207471 intron variant A/G snv 0.20 2
rs11652878
ITGAE
0.925 0.160 17 3751686 missense variant A/C;G snv 4.0E-06; 0.12 2
rs12885526
TSHR ; LOC101928462
0.925 0.160 14 81108085 intron variant G/A snv 0.63 2
rs12756618 1.000 0.160 1 85587205 downstream gene variant C/T snv 4.5E-02 1
rs1393491 1.000 0.160 10 100367390 downstream gene variant T/C snv 0.15 1
rs3917368 1.000 0.160 2 112825205 upstream gene variant C/T snv 0.29 1
rs1264439
ABCF1 ; MIR877
1.000 0.160 6 30584725 intron variant A/C snv 0.74 1
rs1378228
DDAH1
1.000 0.160 1 85570890 intron variant G/C;T snv 1
rs6682848
DDAH1
1.000 0.160 1 85572793 intron variant A/C snv 0.89 1
rs2074505
GNL1
1.000 0.160 6 30553360 synonymous variant G/A snv 0.67 0.66 1
rs1003199
IL12B
1.000 0.160 5 159328558 intron variant C/T snv 0.43 1
rs1057745
MED29
1.000 0.160 19 39397750 missense variant G/A;C snv 1.3E-05; 0.13 1
rs11083522
MIR4530 ; PLEKHG2
1.000 0.160 19 39410971 upstream gene variant T/C snv 0.32 1
rs287084
PDZRN4
1.000 0.160 12 41550605 intron variant T/C snv 1
rs2074503
PRR3
1.000 0.160 6 30562719 3 prime UTR variant T/C snv 0.73 1