Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1163944538
TMEM94
0.641 0.560 17 75494905 frameshift variant -/A delins 4.0E-06 73
rs1352010373
TMEM94
0.641 0.560 17 75489265 splice acceptor variant G/C snv 73
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs1557781252
GATAD2B
0.742 0.320 1 153816414 stop gained G/A snv 33
rs151344517
LOC107985154 ; AFG3L2 ; TUBB6
0.742 0.320 18 12337505 missense variant C/T snv 31
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1555939456
RPS6KA3
0.851 0.200 X 20187956 missense variant T/C snv 21
rs1568523935
SLC25A42
0.776 0.240 19 19105656 stop gained C/G snv 20
rs587778779
CYP27A1
0.807 0.240 2 218814379 splice acceptor variant G/A;T snv 14
rs10766197
CYP2R1
0.807 0.240 11 14900334 upstream gene variant G/A;C snv 6
rs1155563
GC
0.925 0.080 4 71777771 intron variant T/A;C snv 4
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
rs121918237
SLC34A3
0.925 0.240 9 137233234 missense variant G/A;T snv 6.5E-05; 2.7E-05 2
rs1459015 1.000 0.040 11 13500728 upstream gene variant C/A;T snv 1
rs1202430946
IGHMBP2
0.827 0.080 11 68930251 non coding transcript exon variant C/A;T snv 1.4E-05 17
rs2296651
SLC10A1
0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13
rs512555
MS4A2
0.882 0.160 11 60095780 3 prime UTR variant C/A;G;T snv 5.1E-02 3
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2209314
CYP24A1
0.925 0.040 20 54162422 intron variant T/C snv 0.22 2
rs4809957
CYP24A1
0.763 0.240 20 54154632 3 prime UTR variant A/G snv 0.29 10