Disease: Headache
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
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs6296
HTR1B ; LOC105377864
0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 10
rs867770797
EDNRA
0.851 0.200 4 147519875 missense variant G/A snv 8
rs6275
DRD2
0.851 0.160 11 113412755 synonymous variant A/G snv 0.64 0.58 7
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
rs12134493 0.925 0.040 1 115135325 TF binding site variant C/A snv 9.2E-02 4
rs1050316
MEF2D
1 156464911 3 prime UTR variant G/T snv 0.54 3
rs4909945
MRVI1
11 10652192 missense variant T/A;C snv 0.76 2