Disease: Migraine with Aura
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1835740
LOC105375655 ; LOC101927066
0.882 0.040 8 97154685 intergenic variant T/C snv 0.75 5
rs10504861
LOC105375630 ; LOC105375629
0.925 0.040 8 88535703 intron variant C/T snv 0.23 3
rs104894561
CSNK1D
0.882 0.120 17 82265743 missense variant T/C snv 4.0E-06 7.0E-06 5
rs963265
LOC101927086
1.000 0.040 9 70479619 intergenic variant T/C snv 0.36 2
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs12454023
NEDD4L
1.000 0.040 18 58342372 intron variant C/T snv 0.47 2
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 10
rs2137920
VSTM4
1.000 0.040 10 49021593 intron variant T/A snv 0.68 2
rs2074193 1.000 0.040 12 47377646 non coding transcript exon variant T/G snv 0.21 2
rs4379368
SUGCT
0.925 0.040 7 40426601 intron variant C/T snv 0.12 3
rs222741
TRPV1
1.000 0.040 17 3605586 intron variant G/A;C snv 2
rs7217270
TRPV3
1.000 0.040 17 3518181 intron variant A/C;G snv 2
rs2651899
PRDM16 ; LOC105378606
0.882 0.040 1 3167148 intron variant T/A;C snv 5
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs6790925
LOC101927995 ; LOC105377013
0.925 0.040 3 30438593 intergenic variant C/G;T snv 3
rs2066713
SLC6A4
0.807 0.200 17 30224647 intron variant G/A snv 0.34 9
rs1979572
NSRP1
1.000 0.040 17 30184960 synonymous variant G/A snv 0.52 0.49 2
rs2986961 1.000 0.040 10 29798430 regulatory region variant C/T snv 0.65 2
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs2049046
BDNF
0.827 0.200 11 27702228 intron variant T/A snv 0.48 6
rs6741751
TRPM8
0.925 0.040 2 233919016 intron variant G/A snv 7.8E-02 3
rs10166942
TRPM8
0.925 0.040 2 233916448 upstream gene variant T/C snv 0.40 4
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs7015657 1.000 0.040 8 21110040 intron variant C/G snv 0.30 2