Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052553
MAPT
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 8
rs1053924
PPT2-EGFL8 ; LOC100507547 ; PRRT1 ; PPT2
1.000 0.120 6 32152938 non coding transcript exon variant T/C snv 0.71 1
rs1055271
MIOX
1.000 0.120 22 50489911 3 prime UTR variant G/C snv 0.27 1
rs1055569
HCG26 ; HCP5
0.882 0.240 6 31472305 non coding transcript exon variant C/T snv 0.41 3
rs1058026
HLA-B
0.925 0.120 6 31353908 3 prime UTR variant A/C snv 0.21 5
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs1065356
MPIG6B ; LY6G6C
1.000 0.120 6 31719231 synonymous variant G/A snv 0.27 0.31 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
rs10743152
TH
1.000 0.120 11 2174751 upstream gene variant T/C snv 0.63 1
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 8
rs10766196
CYP2R1
0.925 0.120 11 14891585 5 prime UTR variant A/G snv 0.35 2
rs10770125
INS-IGF2 ; IGF2 ; IGF2-AS
0.882 0.200 11 2147784 missense variant A/G snv 0.49 0.40 4
rs10770141
MIR4686 ; TH
1.000 0.120 11 2172610 upstream gene variant A/C;G snv 2
rs1077393
BAG6
0.882 0.200 6 31642752 non coding transcript exon variant A/G snv 0.44 3
rs10774654 1.000 0.120 12 112525756 intergenic variant A/G snv 0.20 1
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs10786436
HPSE2
1.000 0.120 10 98540425 intron variant C/T snv 0.40 1
rs10795791 0.925 0.200 10 6066377 upstream gene variant A/G snv 0.40 2
rs10807113 1.000 0.120 6 32754409 upstream gene variant C/A;G snv 1
rs10810632
BNC2
1.000 0.120 9 16789026 intron variant C/T snv 0.85 1
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs10850053 1.000 0.120 12 112539973 regulatory region variant T/C snv 0.19 1
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40