Disease: Migraine with Aura
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12454023
NEDD4L
1.000 0.040 18 58342372 intron variant C/T snv 0.47 2
rs1979572
NSRP1
1.000 0.040 17 30184960 synonymous variant G/A snv 0.52 0.49 2
rs2074193 1.000 0.040 12 47377646 non coding transcript exon variant T/G snv 0.21 2
rs2137920
VSTM4
1.000 0.040 10 49021593 intron variant T/A snv 0.68 2
rs222741
TRPV1
1.000 0.040 17 3605586 intron variant G/A;C snv 2
rs2820651
ADARB2
1.000 0.040 10 1429570 intron variant C/A snv 0.14 2
rs2986961 1.000 0.040 10 29798430 regulatory region variant C/T snv 0.65 2
rs3761555
GRIA3
1.000 0.040 X 123182584 upstream gene variant T/C snv 0.38 2
rs7015657 1.000 0.040 8 21110040 intron variant C/G snv 0.30 2
rs7217270
TRPV3
1.000 0.040 17 3518181 intron variant A/C;G snv 2
rs963265
LOC101927086
1.000 0.040 9 70479619 intergenic variant T/C snv 0.36 2
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
rs2274316
MEF2D
0.925 0.040 1 156476450 intron variant C/A snv 0.62 0.54 3
rs35737760
CACNA1E
0.925 0.040 1 181732663 missense variant T/A snv 0.13 0.13 3
rs4379368
SUGCT
0.925 0.040 7 40426601 intron variant C/T snv 0.12 3
rs6478241
ASTN2
0.925 0.040 9 116490350 intron variant A/G;T snv 3
rs6741751
TRPM8
0.925 0.040 2 233919016 intron variant G/A snv 7.8E-02 3
rs6790925
LOC101927995 ; LOC105377013
0.925 0.040 3 30438593 intergenic variant C/G;T snv 3
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
rs104894561
CSNK1D
0.882 0.120 17 82265743 missense variant T/C snv 4.0E-06 7.0E-06 5
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
rs2049046
BDNF
0.827 0.200 11 27702228 intron variant T/A snv 0.48 6