Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 8
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 6
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 6
rs12134493 0.925 0.040 1 115135325 TF binding site variant C/A snv 9.2E-02 2
rs1050316
MEF2D
1 156464911 3 prime UTR variant G/T snv 0.54 2
rs4909945
MRVI1
11 10652192 missense variant T/A;C snv 0.76 2
rs8614
NUFIP2
17 29261788 3 prime UTR variant C/A;T snv 2
rs10774231 12 4406208 downstream gene variant T/C snv 0.51 1
rs12740679 1 150289855 upstream gene variant C/G snv 0.25 1
rs34097149 3 154545386 intergenic variant T/C snv 2.0E-02 1
rs4941139 18 62495558 intergenic variant T/C snv 0.31 1
rs7555006 1 51014586 intergenic variant A/G snv 0.48 1
rs9490318 6 121539061 downstream gene variant C/T snv 0.16 1
rs17220352
ASTN2
9 116485780 intron variant A/G snv 0.21 1
rs56349329
ATG13
11 46673933 3 prime UTR variant G/A snv 0.14 1
rs2072806
BTN2A2
1.000 0.040 6 26384865 intron variant C/G snv 7.7E-02 1
rs2895526
CAMK1D
10 12684062 intron variant T/A;G snv 1
rs9486715
FHL5
6 96611893 intron variant A/C snv 0.36 1
rs4596713
FXN
9 69084300 intron variant C/T snv 0.61 1
rs7300001
IFT81
12 110143926 intron variant A/G;T snv 1
rs1518111
IL19 ; IL10
0.790 0.360 1 206771300 intron variant T/C snv 0.71 1
rs1011121
LOC105371345
16 75292035 downstream gene variant A/C;G snv 1
rs1835740
LOC105375655 ; LOC101927066
0.882 0.040 8 97154685 intergenic variant T/C snv 0.75 1
rs56304645
LOC105378606 ; PRDM16
1 3168622 intron variant C/T snv 0.25 1
rs77804065
LOC107985028 ; LINC02210-CRHR1
17 45733530 splice region variant C/A;G;T snv 1