Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs553350297
AGTR1
0.882 0.040 3 148741588 missense variant G/A snv 1.2E-05 2.1E-05 4
rs640198
MMP13
0.851 0.040 11 102954362 intron variant T/G snv 0.68 4
rs7025486
DAB2IP
0.851 0.040 9 121660124 intron variant G/A snv 0.28 4
rs761401927
ACE
0.882 0.040 17 63488704 missense variant G/A snv 9.1E-05 4
rs762079672
AGT
0.882 0.040 1 230710211 missense variant C/T snv 4.0E-06 4
rs897876 0.882 0.040 2 65564447 intron variant C/T snv 0.30 4
rs10159239
NLRP3
0.882 0.040 1 247443750 intron variant G/A snv 0.57 3
rs1051339
LIPA
0.882 0.040 10 89247582 missense variant C/T snv 9.5E-02 0.13 3
rs10918859
NOS1AP
0.882 0.040 1 162199478 intron variant G/A snv 0.16 3
rs12040273
GALNT2
0.882 0.040 1 230063651 intron variant C/T snv 0.28 3
rs12115090
CRISPLD1
0.882 0.040 8 75012585 intron variant A/C snv 0.33 0.44 3
rs12344245
FAM189A2
0.882 0.040 9 69340801 intron variant A/G snv 0.12 3
rs12704673
CALCR
0.882 0.040 7 93525009 intron variant A/G;T snv 0.27 3
rs1351855165
DUOX2
0.882 0.040 15 45111550 synonymous variant G/A snv 3
rs138760780
CDK18
0.882 0.040 1 205515245 intron variant C/T snv 1.5E-02 3
rs1411364031
TNF
0.882 0.040 6 31577502 missense variant T/C snv 7.0E-06 3
rs141383962
CLU
0.882 0.040 8 27605112 missense variant C/G;T snv 7.2E-05 1.0E-04 3
rs1433748662
KIDINS220
0.882 0.040 2 8791221 missense variant T/C snv 3
rs145297799
NPC1L1
0.882 0.040 7 44539181 stop gained G/A snv 9.1E-05 9.8E-05 3
rs16941382
GOSR2 ; LRRC37A2
0.882 0.040 17 46966142 intron variant T/C snv 0.15 3
rs16998248
ZNF217
0.882 0.040 20 53581801 synonymous variant T/A snv 0.11 8.8E-02 3
rs189970623
CYP2B6
0.882 0.040 19 41009368 missense variant C/A;G;T snv 3.0E-04 3
rs2254638
N6AMT1
0.882 0.040 21 28883961 intron variant A/C;G snv 3
rs2267788
LOC105371077 ; GRIN2A
0.882 0.040 16 9794742 intron variant C/T snv 3
rs2870463 0.882 0.040 16 75216819 upstream gene variant G/A snv 0.14 3