Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs221798
GIGYF1
0.882 0.040 7 100689872 intron variant C/A;G snv 3
rs221774 0.851 0.080 7 100701361 upstream gene variant A/G;T snv 4
rs506597 0.882 0.040 7 100715797 upstream gene variant A/G snv 0.90 4
rs12426318
HELLPAR
1.000 0.040 12 102241743 non coding transcript exon variant C/A snv 0.18 1
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40 5
rs11487077
NAPEPLD
1.000 0.040 7 103105631 intron variant A/C snv 6.5E-02 1
rs6465903
NAPEPLD
1.000 0.040 7 103134811 intron variant C/A snv 0.13 1
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs362719
RELN
0.925 0.040 7 103545430 intron variant C/A snv 0.32 2
rs6484218
CAND1.11 ; AMPD3
0.882 0.040 11 10369034 intron variant G/A snv 0.21 5
rs7337127 0.925 0.080 13 104623579 intergenic variant C/A;T snv 2
rs12669727
LHFPL3 ; LHFPL3-AS1
1.000 0.040 7 104776829 intron variant T/A;C snv 1
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs1130214
AKT1
0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs3803300
ZBTB42
0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs735931
ATP2B2
1.000 0.040 3 10483412 intron variant A/G snv 0.60 1
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs73188321 1.000 0.040 7 105407711 intergenic variant C/T snv 0.35 1
rs3916966 0.882 0.080 13 105458546 upstream gene variant C/A snv 0.63 4
rs3916967
DAOA-AS1 ; DAOA
0.882 0.040 13 105464999 intron variant T/C snv 0.32 3
rs2391191
DAOA-AS1 ; DAOA
0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 7
rs3918341
DAOA ; DAOA-AS1
1.000 0.040 13 105468070 intron variant A/G snv 0.34 1
rs1935062
DAOA ; DAOA-AS1
0.882 0.080 13 105475787 intron variant A/C snv 0.32 3
rs9558571
DAOA-AS1 ; DAOA
0.882 0.040 13 105486017 intron variant C/T snv 0.28 3