Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10305650
ARNT
1 150876501 intron variant G/A;C snv 1.3E-02 2
rs10305685
ARNT
1 150838529 intron variant T/C snv 5.4E-02 2
rs1031045
LPL
8 19943601 intron variant G/A snv 0.12 3
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 7
rs1037116 15 101528701 upstream gene variant C/T snv 0.20 2
rs1037378
PDE3B
11 14830944 intron variant G/A snv 0.52 1
rs1038026
TOMM40
1.000 0.080 19 44901805 3 prime UTR variant A/G;T snv 4
rs10401176
BCL3
1.000 0.080 19 44750234 intron variant C/G;T snv 0.17 2
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs10402729
NCAN
19 19244291 intron variant T/C snv 3.3E-02 4
rs10405178
SLC25A42
19 19064943 intron variant T/G snv 2.5E-02 2
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs10411413
SUGP2
19 19009572 intron variant C/T snv 2.4E-02 2
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 6
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs10422058
ARMC6
19 19047391 intron variant T/A;C snv 2
rs10426401
LOC107985305 ; PVR
1.000 0.080 19 44644419 intron variant T/G snv 0.32 2
rs10427943
CABIN1
22 24131331 intron variant G/T snv 1.2E-02 2
rs10438978
LOC105372112
18 49631816 intergenic variant T/C snv 0.75 2
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 6
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs10478730
EDN1
6 12297276 downstream gene variant C/T snv 1.2E-02 5
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs10479024 5 133131681 intergenic variant C/A;T snv 1