Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7296503
PDZRN4
12 41306962 intron variant C/T snv 0.57 13
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs10821907 0.776 0.080 10 50888694 upstream gene variant C/T snv 0.20 12
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 10
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7