Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs1275805226
AGT
0.776 0.240 1 230706148 frameshift variant G/- del 7.0E-06 12
rs2740574
CYP3A4
0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78 12
rs2016347
IGF1R
0.790 0.160 15 98960571 3 prime UTR variant G/A;T snv 9
rs2074192
ACE2
0.827 0.160 X 15564667 intron variant C/T snv 0.40 9
rs2070584
TIMP1 ; MIR4769 ; SYN1
0.790 0.200 X 47587120 intron variant T/G snv 0.44 8
rs2779249
NOS2
0.851 0.200 17 27801555 intron variant C/A snv 0.33 7
rs3957357
GSTA1
0.807 0.280 6 52803889 upstream gene variant A/G snv 0.63 7
rs846910
HSD11B1 ; HSD11B1-AS1
0.882 0.160 1 209701909 intron variant A/G snv 0.95 6
rs2881766
ESR1
0.882 0.120 6 151797984 intron variant T/G snv 0.35 5
rs41511344
NR3C2
0.882 0.040 4 148152550 stop gained G/A;T snv 5
rs1319501
NAMPT
0.882 0.120 7 106285307 intron variant C/A;T snv 0.76 4
rs2235543
HSD11B1-AS1 ; HSD11B1
0.925 0.080 1 209687323 intron variant T/A;C snv 4
rs3801266
NAMPT
0.925 0.080 7 106283804 intron variant T/C snv 0.26 3
rs1643821
ESR1
6 151862416 intron variant G/A snv 0.46 2
rs2234681
MMP9
1.000 0.040 20 46008773 upstream gene variant ACACACACACACACACACACACAC/-;AC;ACAC;ACACAC;ACACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC;ACACACACACACACAC;ACACACACACACACACAC;ACACACACACACACACACAC;ACACACACACACACACACACAC;ACACACACACACACACACACACACAC;ACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACACACAC delins 2
rs10458894
STIM1
11 3892042 intron variant T/A;C snv 1
rs11466414
TGFB3 ; IFT43
14 75981507 non coding transcript exon variant G/A snv 4.7E-02 1
rs12710567
AGTR2
X 116170599 upstream gene variant T/C snv 3.2E-02 1
rs7945554
STIM1
11 3857748 intron variant G/A snv 0.37 1