Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2974935
MTX1
0.708 0.280 1 155212052 non coding transcript exon variant G/A;C;T snv 17
rs481519
NEK10
0.708 0.280 3 27285723 intron variant C/A;T snv 17
rs11844632
RAD51B
0.708 0.280 14 68559662 intron variant G/A snv 0.23 17
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv 17
rs7725218
TERT
0.708 0.280 5 1282299 intron variant G/A snv 0.38 17
rs11168936
TUBA1C
0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
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
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 15
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 13
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 11
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 11
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 11
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs2735940
TERT
0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 10
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 9
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 9
rs12241008
VTI1A
0.716 0.160 10 112520943 intron variant T/C snv 0.13 9
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs56113850
CYP2A6
0.807 0.080 19 40847202 intron variant T/C snv 0.52 8
rs35789010
CARMIL1
0.851 0.200 6 25513951 intron variant G/A snv 4.1E-02 7