Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs61755320
SPG7
0.716 0.520 16 89546737 missense variant C/T snv 2.9E-03 3.5E-03 41
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs2234767
FAS ; ACTA2
0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs763110
FASLG
0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs4633
COMT ; MIR4761
0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 25
rs143383
GDF5
0.724 0.320 20 35438203 5 prime UTR variant G/A snv 0.47 17
rs11200638
LOC105378525 ; HTRA1
0.724 0.280 10 122461028 non coding transcript exon variant G/A snv 0.23 14
rs1800012
COL1A1
0.763 0.320 17 50200388 intron variant C/A snv 0.14 13
rs2073711
CILP
0.807 0.160 15 65201874 missense variant A/G snv 0.56 0.61 7
rs5030772
FASLG
0.790 0.320 1 172664210 intron variant A/G snv 9.9E-02 7
rs77245812
MATN3 ; LOC101928222
0.882 0.040 2 20003169 missense variant G/A snv 1.5E-02 1.2E-02 3
rs1793953
COL2A1
0.925 0.080 12 47999743 non coding transcript exon variant G/A snv 0.53 2
rs2276454
COL2A1 ; LOC105369752
0.925 0.040 12 47982508 synonymous variant G/A snv 0.39 0.38 2
rs11076008
FTO
0.925 0.120 16 53893411 intron variant G/A;C snv 2
rs201621853
IGFBP6
0.925 0.040 12 53100807 missense variant T/C snv 1.2E-05 2
rs10046257 1.000 0.040 6 32886920 regulatory region variant G/A snv 0.15 1
rs10214886 1.000 0.040 6 32889642 intergenic variant T/A snv 0.14 1