Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1459015 1.000 0.040 11 13500728 upstream gene variant C/A;T snv 1
rs2246709
CYP3A4
1.000 0.040 7 99768096 intron variant A/G snv 0.31 1
rs2209314
CYP24A1
0.925 0.040 20 54162422 intron variant T/C snv 0.22 2
rs10766196
CYP2R1
0.925 0.120 11 14891585 5 prime UTR variant A/G snv 0.35 2
rs121918237
SLC34A3
0.925 0.240 9 137233234 missense variant G/A;T snv 6.5E-05; 2.7E-05 2
rs1428826948
APOL1
0.925 0.040 22 36265940 synonymous variant T/G snv 1.2E-05 3
rs1569534160
APOL1
0.925 0.040 22 36265812 missense variant A/G snv 3
rs512555
MS4A2
0.882 0.160 11 60095780 3 prime UTR variant C/A;G;T snv 5.1E-02 3
rs4809959
CYP24A1
0.851 0.200 20 54169320 intron variant A/G snv 0.51 4
rs1155563
GC
0.925 0.080 4 71777771 intron variant T/A;C snv 4
rs2242480
CYP3A4
0.882 0.120 7 99763843 intron variant C/T snv 0.22 0.32 5
rs10766197
CYP2R1
0.807 0.240 11 14900334 upstream gene variant G/A;C snv 6
rs1993116
CYP2R1
0.827 0.200 11 14888688 intron variant A/G snv 0.65 8
rs2239179
VDR
0.790 0.200 12 47863983 intron variant T/C snv 0.39 9
rs4809957
CYP24A1
0.763 0.240 20 54154632 3 prime UTR variant A/G snv 0.29 10
rs2060793
CYP2R1
0.776 0.240 11 14893764 upstream gene variant A/G snv 0.63 11
rs2296651
SLC10A1
0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13
rs587778779
CYP27A1
0.807 0.240 2 218814379 splice acceptor variant G/A;T snv 14
rs4646536
CYP27B1
0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 14
rs12794714
CYP2R1
0.708 0.360 11 14892029 synonymous variant G/A snv 0.41 0.35 15
rs1202430946
IGHMBP2
0.827 0.080 11 68930251 non coding transcript exon variant C/A;T snv 1.4E-05 17
rs1568523935
SLC25A42
0.776 0.240 19 19105656 stop gained C/G snv 20
rs1555939456
RPS6KA3
0.851 0.200 X 20187956 missense variant T/C snv 21
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25