Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3094122 1.000 0.120 6 30760583 intron variant T/G snv 0.21 1
rs3104402 1.000 0.120 6 32713899 upstream gene variant T/G snv 0.96 1
rs3842753
INS-IGF2 ; INS
1.000 0.120 11 2159830 missense variant T/G snv 0.73 0.60 1
rs4849135
ACOXL
1.000 0.120 2 110857502 intron variant T/G snv 0.67 1
rs7762619
LTA ; LOC100287329
1.000 0.120 6 31563533 downstream gene variant T/G snv 1.5E-02 1
rs928815
LOC100287329 ; LTA
1.000 0.120 6 31563438 downstream gene variant T/G snv 0.65 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs9261290
RNF39
0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs9273349
HLA-DQB1-AS1
0.827 0.200 6 32658092 upstream gene variant T/C;G snv 6
rs1150752
TNXB
0.882 0.240 6 32096949 missense variant T/C;G snv 5.9E-02 3
rs412657 0.882 0.240 6 32243308 intergenic variant T/C;G snv 3
rs7202877 0.882 0.160 16 75213347 intergenic variant T/C;G snv 3
rs2050189
TSBP1 ; TSBP1-AS1
0.925 0.200 6 32371870 5 prime UTR variant T/C;G snv 0.18 2
rs272893
SLC22A4 ; MIR3936HG
0.925 0.160 5 132327369 missense variant T/C;G snv 0.58; 4.0E-06 2
rs35795399
ART3 ; CXCL10
1.000 0.120 4 76021524 3 prime UTR variant T/C;G snv 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs3804100
TLR2
0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs12976445
SPACA6 ; SPACA6P-AS ; MIRLET7E ; MIR125A
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45 20
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18