Disease: Common Migraine
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
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs2236225
MTHFD1
0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs2890565
UTS2
0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 15
rs228648
UTS2
0.776 0.360 1 7853370 missense variant G/A snv 0.51 0.52 13
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs1950902
MTHFD1
0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 10
rs2271933
HCRTR1
0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50 9
rs2049046
BDNF
0.827 0.200 11 27702228 intron variant T/A snv 0.48 6
rs1835740
LOC105375655 ; LOC101927066
0.882 0.040 8 97154685 intergenic variant T/C snv 0.75 5
rs2651899
PRDM16 ; LOC105378606
0.882 0.040 1 3167148 intron variant T/A;C snv 5
rs10166942
TRPM8
0.925 0.040 2 233916448 upstream gene variant T/C snv 0.40 4
rs12134493 0.925 0.040 1 115135325 TF binding site variant C/A snv 9.2E-02 4
rs3754701
RAMP1
0.882 0.120 2 237858561 upstream gene variant A/C;T snv 4
rs10504861
LOC105375630 ; LOC105375629
0.925 0.040 8 88535703 intron variant C/T snv 0.23 3
rs2195450
GRIA1
0.925 0.040 5 153491449 intron variant G/A snv 0.17 3