Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80292941
CYTOR ; LOC101928152
1.000 0.040 2 87480257 non coding transcript exon variant A/T snv 0.16 2
rs7932766
TIRAP
0.925 0.080 11 126292967 synonymous variant C/T snv 0.18 0.19 2
rs7842342
LY96
1.000 0.040 8 73990877 upstream gene variant T/A snv 7.0E-06 1
rs7832767
SFRP1
1.000 0.040 8 41302340 intron variant C/T snv 1.0E-01 1
rs7813
GEMIN4
0.689 0.360 17 744946 missense variant G/A;C snv 0.63 22
rs779826162
TLR1
0.925 0.080 4 38796574 missense variant C/T snv 2.0E-05 1.4E-05 2
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs7749390
IFNGR1
0.882 0.120 6 137219233 5 prime UTR variant A/G;T snv 0.43; 4.4E-06 3
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs772717932
IL1B
1.000 0.040 2 112830530 missense variant C/A;T snv 4.0E-06; 1.6E-05 2
rs7675690
EREG
1.000 0.040 4 74382934 intron variant A/G snv 9.3E-02 1
rs76600635
TLR1
0.925 0.040 4 38798702 missense variant A/G snv 8.2E-03 2.8E-03 3
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs7559955
MARCO
1.000 0.040 2 118967393 intron variant C/G;T snv 1
rs755850200
VDR
1.000 0.040 12 47846347 missense variant T/C snv 2.1E-05 7.0E-06 2
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs755508039
MAS1
1.000 0.040 6 159907236 missense variant A/C;G snv 1
rs755017
ZBTB46
0.925 0.080 20 63790269 synonymous variant A/C;G snv 0.17 2
rs754342091
TLR4
0.790 0.200 9 117712421 missense variant A/G snv 3.2E-05 1.4E-05 7
rs751683612
SLC11A1
1.000 0.040 2 218394932 missense variant C/T snv 4.0E-06 7.0E-06 1
rs751273816
CMPK1
1.000 0.040 1 47373057 missense variant G/A snv 4.0E-06 1
rs748009686
IFNA10
0.925 0.080 9 21206547 missense variant C/A;G snv 2.0E-05; 4.0E-06 2
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 10
rs735240
CD209
0.851 0.360 19 7748450 upstream gene variant G/A snv 0.40 4