Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1982073
TGFB1
0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs2073618
COLEC10 ; TNFRSF11B
0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 19
rs3087456
CIITA ; LOC105371080
0.742 0.480 16 10877045 intron variant G/A snv 0.53 14
rs1800012
COL1A1
0.763 0.320 17 50200388 intron variant C/A snv 0.14 13
rs3736228
LRP5
0.752 0.400 11 68433827 missense variant C/T snv 0.13 0.11 13
rs1800544
ADRA2A
0.790 0.160 10 111076745 upstream gene variant G/C snv 0.59 12
rs3102735
COLEC10 ; TNFRSF11B
0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 12
rs3134069
COLEC10 ; TNFRSF11B
0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
rs13182402
ALDH7A1
0.925 0.160 5 126582456 intron variant A/G snv 0.15 4
rs6831280
IDUA
0.925 0.080 4 1002377 missense variant G/A;C snv 0.17 4
rs587777005
LGR4
0.925 0.120 11 27391119 stop gained G/A snv 1.4E-05 4
rs2908004
WNT16
1.000 0.040 7 121329715 missense variant G/A;T snv 0.44; 4.0E-06 4
rs3917
COL1A2
0.925 0.160 7 94431047 3 prime UTR variant -/GCTGTCC;GTTG;GTTGTCC;GTTGTGC ins 3
rs3102734
COLEC10 ; TNFRSF11B
0.925 0.080 8 118951777 intron variant G/A snv 7.3E-02 9.5E-02 3
rs1107748
LINC02594
1.000 0.080 17 43696446 intron variant T/C snv 0.54 3
rs10085588
LOC105375412 ; SEM1 ; LOC105375411
1.000 0.080 7 96508362 intron variant A/G snv 0.72 3
rs281865264
BEST1 ; LOC107984334
1.000 0.080 11 61959539 missense variant T/A;C snv 4.0E-06 2
rs758488397
COL1A2
1.000 0.080 7 94412666 missense variant G/A;C snv 2
rs6469804
COLEC10
8 119032590 intron variant G/A;C snv 2