Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs3925584
LOC101928338
1.000 0.080 11 30738788 intergenic variant T/C snv 0.35 7
rs77924615
PDILT
1.000 0.080 16 20381010 intron variant G/A snv 0.16 7
rs12423664
FBRSL1
1.000 0.040 12 132493308 intron variant G/A snv 0.10 6
rs13241427 1.000 7 1249003 regulatory region variant G/T snv 0.72 6
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 5
rs12801636
PCNX3
1.000 0.040 11 65623846 intron variant G/A snv 0.25 5
rs174455
FADS3
1.000 0.080 11 61888645 intron variant G/A;C snv 5
rs626277
DACH1
1.000 0.080 13 71773564 intron variant A/C snv 0.51 5
rs11066453
OAS1
1.000 0.080 12 112927816 intron variant A/G snv 3.8E-03 4
rs11554266
GNAS
1.000 0.040 20 58903791 splice region variant C/G;T snv 4.0E-06; 2.3E-03 4
rs138551969
VEGFA
1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05 4
rs187355703
HOXD-AS2 ; LOC100129455 ; HOXD8
1.000 0.080 2 176128855 intron variant C/G snv 1.5E-02 1.5E-02 4
rs201874364
ETV5
1.000 0.040 3 186065822 missense variant C/A;T snv 4.0E-06; 7.2E-05 4
rs202007714
SLC25A26 ; LRIG1
1.000 0.040 3 66383098 missense variant G/A;C snv 1.4E-04; 4.0E-06 4
rs35258188
WDR72
1.000 0.040 15 53705141 missense variant T/G snv 3.5E-03 1.5E-02 4
rs73728279
PRKAG2
1.000 0.080 7 151714408 intron variant G/A;T snv 4
rs10223666
LOC105375069 ; LOC107986598
1.000 0.040 6 43837765 intron variant G/A;C snv 3
rs11949767
MXD3
1.000 0.080 5 177313243 upstream gene variant A/C;G snv 3
rs13226650
MLXIPL
1.000 0.040 7 73602675 intron variant A/G snv 0.19 3
rs13230625 1.000 0.080 7 1246608 regulatory region variant G/A snv 0.62 3
rs142085340
SIPA1L3
1.000 0.080 19 38106538 splice region variant C/T snv 9.1E-05 3.0E-04 3
rs143231463
RREB1
1.000 0.040 6 7226577 missense variant A/G snv 1.8E-04 2.1E-04 3
rs151305324
TMEM171
1.000 0.040 5 73123606 missense variant G/A snv 6.8E-05; 8.0E-06 9.1E-05 3