Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4795397
ZPBP2
0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38 4
rs259964
ZNF831
0.827 0.120 20 59249254 intron variant A/G;T snv 6
rs17800987
ZNF300P1
5 150943866 non coding transcript exon variant A/G snv 0.14 0.13 1
rs11741861
ZNF300 ; IRGM
0.925 0.040 5 150898347 intron variant A/G snv 8.8E-02 3
rs1250550
ZMIZ1
0.851 0.240 10 79300560 intron variant C/A snv 0.27 5
rs1250546
ZMIZ1
0.925 0.080 10 79272775 intron variant A/G snv 0.36 3
rs1250569
ZMIZ1
0.925 0.040 10 79285450 intron variant T/C snv 0.44 0.51 3
rs1250566
ZMIZ1
10 79286696 intron variant G/A snv 0.24 1
rs2315008
ZGPAT
0.925 0.120 20 63712604 intron variant T/G snv 0.70 4
rs6062504
ZGPAT
0.925 0.040 20 63717555 intron variant A/G;T snv 3
rs35873774
XBP1
0.925 0.040 22 28795944 intron variant A/G snv 4.6E-02 3
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18 9
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18 7
rs9557207
UBAC2
13 99384164 intron variant A/G snv 0.17 2
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs35018800
TYK2
0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 9
rs1292053
TUBD1
1.000 0.040 17 59886176 missense variant A/G snv 0.45 0.46 2
rs7097656
TSPAN14
0.827 0.120 10 80491075 intron variant T/C;G snv 6
rs6586030
TSPAN14
1.000 0.040 10 80494291 intron variant A/G;T snv 2
rs9471535
TREM1
0.851 0.240 6 41287752 upstream gene variant T/C snv 0.12 5
rs2179070
TRAF3IP2-AS1 ; TRAF3IP2
6 111564549 intron variant T/C;G snv 1
rs1142345
TPMT
0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 9