Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1052553
MAPT
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 8
rs1059174
HLA-F-AS1 ; HLA-F
1.000 0.080 6 29726650 non coding transcript exon variant C/A;T snv 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1061581
HSPA1A ; HSPA1L
0.827 0.200 6 31816809 synonymous variant G/A snv 6
rs1064395
NCAN
0.882 0.120 19 19250926 3 prime UTR variant G/A snv 0.24 3
rs10735781
EVI5
1.000 0.080 1 92655550 intron variant G/C snv 0.57 1
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs1077667
TNFSF14
0.925 0.120 19 6668961 intron variant C/G;T snv 2
rs10797431
LOC100996583
0.851 0.080 1 2569783 non coding transcript exon variant G/T snv 0.42 5
rs10800309 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 3
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 6
rs10807344
SLC25A27
0.925 0.120 6 46657898 intron variant C/T snv 0.17 2
rs10823051
CTNNA3
1.000 0.080 10 67504839 intron variant G/C snv 0.13 1
rs10866713 1.000 0.080 5 159491886 intron variant G/A snv 0.16 1
rs10876994 0.925 0.120 12 57670954 upstream gene variant A/C;T snv 2
rs10877013
METTL1 ; EEF1AKMT3
1.000 0.080 12 57771302 intron variant C/T snv 0.38 0.32 1
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs10984447
BRINP1
1.000 0.080 9 119222275 intron variant A/G snv 0.19 1