Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs121918455
PTPN11
0.695 0.440 12 112477720 missense variant A/C;G snv 31
rs12041331
PEAR1
0.776 0.200 1 156899922 intron variant G/A snv 0.19 11
rs2516400 0.827 0.320 6 31513328 upstream gene variant G/A snv 0.32 8
rs4523
TBXA2R
0.776 0.280 19 3595796 missense variant A/G snv 0.56 0.66 8
rs5050
AGT
0.827 0.200 1 230714140 intron variant T/C;G snv 7
rs2229634
ITPR3
0.851 0.240 6 33670403 synonymous variant C/A;T snv 4.0E-06; 0.33 4
rs899162 0.882 0.160 5 135459219 downstream gene variant G/A snv 1.0E-01 3
rs16921209
LOC102725112 ; NEBL
0.882 0.160 10 20879174 intron variant C/G snv 4.6E-02 3
rs7637803
MED12L ; P2RY12
0.882 0.160 3 151371438 intron variant C/G;T snv 3
rs17076896
TUBA3C ; LOC101928697
0.882 0.160 13 19181923 upstream gene variant T/C snv 8.3E-02 3
rs10127456
FHAD1 ; FHAD1-AS1
0.925 0.120 1 15327376 non coding transcript exon variant G/A snv 0.25 2
rs17136627
LOC101927078 ; KCNN2
0.925 0.120 5 114463289 intron variant C/T snv 7.5E-02 2
rs12210919
MDGA1
0.925 0.120 6 37677736 intron variant T/C snv 6.8E-02 2
rs12900413
MESP2
0.925 0.120 15 89777808 intron variant A/G snv 0.27 2
rs17782904
SETBP1
0.925 0.120 18 44733745 intron variant G/A snv 0.18 2
rs11793049
ZNF618
0.925 0.120 9 114011589 intron variant A/G;T snv 2