Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs1800012
COL1A1
0.763 0.320 17 50200388 intron variant C/A snv 0.14 13
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 12
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53 8
rs2239185
VDR
0.807 0.320 12 47850776 intron variant G/A snv 0.54 6
rs2047937
ZNF423
0.925 0.120 16 49830880 intron variant C/T snv 0.50 5
rs3130340
TSBP1-AS1
0.851 0.200 6 32276850 intron variant T/C snv 0.25 5
rs1038304
CCDC170 ; LOC107986528
0.882 0.160 6 151612040 intron variant A/G snv 0.58 4
rs13182402
ALDH7A1
0.925 0.160 5 126582456 intron variant A/G snv 0.15 4
rs1800247
BGLAP ; PMF1-BGLAP
0.882 0.200 1 156242034 intron variant T/C snv 0.20 4
rs2420946
FGFR2
0.851 0.160 10 121591810 intron variant T/C snv 0.56 4
rs749292
CYP19A1 ; MIR4713HG
0.851 0.160 15 51266534 intron variant G/A snv 0.44 4
rs7776725
FAM3C
1.000 0.080 7 121393067 intron variant T/C snv 0.28 4
rs10085588
LOC105375412 ; SEM1 ; LOC105375411
1.000 0.080 7 96508362 intron variant A/G snv 0.72 3
rs2273061
JAG1
1.000 0.080 20 10658895 intron variant G/A snv 0.46 3
rs3102734
COLEC10 ; TNFRSF11B
0.925 0.080 8 118951777 intron variant G/A snv 7.3E-02 9.5E-02 3
rs3782905
VDR
0.882 0.200 12 47872384 intron variant G/C snv 0.29 3
rs4870044
CCDC170
1.000 0.080 6 151580274 intron variant C/T snv 0.44 3
rs12585014
TNFSF11
1.000 0.080 13 42566423 intron variant G/A snv 0.18 2