Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1663564
WASHC4
12 105152394 missense variant G/A snv 0.95 0.95 1
rs6297
LOC105377864 ; HTR1B
6 77462224 3 prime UTR variant C/A;T snv 0.89 1
rs2383101
SLC24A2
9 19576951 missense variant T/A;G snv 8.0E-06; 0.84 1
rs890076
TBR1
2 161424237 3 prime UTR variant G/A;C snv 0.82 1
rs1041073
B3GLCT
13 31317609 missense variant G/A snv 0.75 0.66 1
rs345736
EPHA7
6 93254601 intron variant C/T snv 0.75 0.76 1
rs2518907
NRXN2
11 64713169 synonymous variant G/A;C snv 0.69 1
rs4939208
OR5B17
11 58358832 missense variant A/T snv 0.69 0.67 1
rs1060709
B3GLCT
13 31329697 3 prime UTR variant G/A;T snv 1.2E-05; 0.64 1
rs3748400
ZCCHC14
16 87412233 missense variant C/T snv 0.64 0.57 1
rs1131017
RPS26 ; LOC105369780
0.925 0.160 12 56042145 5 prime UTR variant C/A;G;T snv 8.0E-06; 8.0E-06; 0.62; 1.1E-04 3
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 4
rs1051860
LOC105370522 ; ARID4A
14 58371950 synonymous variant A/G snv 0.58 0.54 1
rs133885
MYO18B
1.000 0.120 22 25763322 missense variant G/A;C snv 0.55 1
rs3808964
GPR26
10 123667111 intron variant G/T snv 0.53 0.52 1
rs1614887
BTN2A2
6 26392793 synonymous variant G/A snv 0.53 0.63 2
rs2279574
DUSP6
0.827 0.120 12 89351700 missense variant C/A;T snv 0.52 1
rs112422823
CYHR1 ; KIFC2
8 144466532 intron variant G/C;T snv 0.48; 1.0E-04 1
rs3801057
FBXL18
7 5491196 intron variant G/A snv 0.48 0.48 1
rs9416018
DNAJB12
10 72340884 intron variant G/A snv 0.47 0.43 1
rs10122976
KCNT1
9 135751066 intron variant C/A;T snv 0.47; 1.2E-05 1
rs204883
TNXB
1.000 0.120 6 32064966 missense variant G/A;C snv 0.44 1
rs2240715
ARVCF
22 19973083 intron variant G/C snv 0.39 0.44 1
rs878756
MRTFA
22 40418496 missense variant T/C;G snv 0.38 1
rs10783299
DDN-AS1 ; DDN
12 48996894 missense variant T/C snv 0.38 0.42 1