Disease: Atherosclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs746481995
HSD11B1 ; HSD11B1-AS1
0.882 0.120 1 209707123 missense variant T/C snv 4.0E-06 3
rs750805885
MCL1 ; LOC107985203
0.882 0.080 1 150579475 frameshift variant -/C delins 4.7E-06 3
rs7629265
SCN5A
0.882 0.080 3 38607330 intron variant C/T snv 2.3E-02 3
rs7833904 0.882 0.040 8 58505103 upstream gene variant A/T snv 0.55 3
rs79681911
SAA1
0.882 0.040 11 18269755 missense variant G/A snv 2.1E-03 8.0E-04 3
rs8042271 0.882 0.040 15 89030987 intergenic variant G/A;T snv 3
rs8070488
HGS
0.882 0.080 17 81696901 synonymous variant T/C snv 0.21 0.26 3
rs121918313
LRP6 ; BCL2L14
0.851 0.080 12 12164494 missense variant G/A snv 1.6E-05 4
rs12762303
ALOX5
0.851 0.080 10 45373723 upstream gene variant T/C snv 0.17 4
rs1298417395
COP1
0.882 0.080 1 176206716 missense variant C/T snv 1.4E-05 4
rs1440763451
PPARG
0.882 0.080 3 12416849 missense variant A/G snv 4.0E-06 4
rs1867624 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 4
rs200222843
APOB
0.851 0.120 2 21003286 missense variant G/A snv 4.0E-05 4.2E-05 4
rs243330
SOCS1 ; RMI2 ; LOC105371082
0.851 0.240 16 11257134 intron variant C/T snv 0.49 4
rs2518136
AHSG
0.851 0.120 3 186620038 intron variant T/C snv 0.46 4
rs33932899
LOC105371082 ; RMI2 ; SOCS1
0.851 0.240 16 11254354 intron variant C/G;T snv 4
rs3736234
OLR1
0.851 0.040 12 10160535 non coding transcript exon variant G/A snv 0.40 4
rs4845617
IL6R-AS1 ; IL6R
0.882 0.080 1 154405422 5 prime UTR variant G/A;C snv 4
rs4845623
IL6R
0.925 0.040 1 154443301 intron variant A/G snv 0.47 4
rs4862423
ACSL1
0.882 0.080 4 184805394 intron variant C/T snv 0.37 4
rs4987262
PTGIR
0.882 0.040 19 46623592 missense variant G/A;C snv 7.1E-03 4
rs755460305
KNG1
0.882 0.080 3 186732650 missense variant C/A snv 4
rs755725121
PIK3CD
0.882 0.080 1 9716029 missense variant G/A snv 2.1E-05 7.0E-06 4
rs773297988
PIK3CB
0.882 0.080 3 138698965 missense variant T/C snv 4.0E-06 3.5E-05 4
rs774887459
SGSM3
0.882 0.080 22 40405776 missense variant G/A snv 4.0E-06 4