Disease: Arteriosclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10846744
SCARB1
0.763 0.160 12 124827879 intron variant G/C snv 0.32 11
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs12564445
TNNT2
0.851 0.040 1 201376359 intron variant G/A snv 0.27 5
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs13447720
MRE11
0.925 0.040 11 94432160 intron variant T/C snv 0.17 2
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1535045
CD40
0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs17228212
SMAD3
0.807 0.160 15 67166301 intron variant T/C snv 0.21 8
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs212528
ECE1
0.925 0.040 1 21259168 intron variant T/C snv 0.12 3
rs213045
ECE1
0.851 0.120 1 21290752 intron variant G/T snv 0.44 5
rs2144908
LOC105372629 ; HNF4A
0.851 0.120 20 44357077 intron variant G/A snv 0.18 5
rs2269422
AGER
0.882 0.040 6 32183517 intron variant T/C snv 1.7E-02 5.8E-03 3
rs243330
SOCS1 ; RMI2 ; LOC105371082
0.851 0.240 16 11257134 intron variant C/T snv 0.49 4
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs2518136
AHSG
0.851 0.120 3 186620038 intron variant T/C snv 0.46 4