Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 16
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 15
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 10
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 9
rs9392504 0.827 0.120 6 412802 downstream gene variant G/A snv 0.44 7
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 7
rs9880772 0.827 0.240 3 27736288 intergenic variant G/A snv 0.59 5
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 5
rs4459895
LPP
0.827 0.160 3 188236626 intron variant A/C snv 0.88 5
rs6793295
LRRC34
0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 5
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 5
rs4240807 0.851 0.160 16 85951755 downstream gene variant A/C snv 0.76 4
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 4
rs9392017 0.851 0.160 6 442357 intergenic variant G/A;C snv 4
rs35603048
BMF
0.851 0.160 15 40099764 intron variant C/A;G;T snv 4
rs73005220
CIB3
0.851 0.160 19 16161878 intron variant A/G snv 3.9E-02 4
rs806321
DLEU1
0.851 0.160 13 50267187 intron variant C/T snv 0.47 4
rs6546149
DTNB
0.851 0.160 2 25406569 intron variant C/G snv 0.38 4
rs2546191
ELL2
0.851 0.160 5 95896837 intron variant G/A snv 0.38 4
rs3755397
FARP2
0.925 0.120 2 241355498 upstream gene variant A/G snv 6.8E-02 4
rs4525246
GRAMD1B
0.851 0.160 11 123524538 intron variant G/A;C snv 4
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs9391997
IRF4
0.851 0.160 6 409119 3 prime UTR variant A/G snv 0.38 4
rs181181503
LOC100507377
0.851 0.160 12 74276187 intron variant T/C snv 1.5E-03 4