Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1200399
BAZ1A
0.925 0.080 14 34823979 intron variant C/T snv 0.87 2
rs1571228
SAXO1
1.000 0.080 9 18930224 intron variant G/A snv 0.83 1
rs1950902
MTHFD1
0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 1
rs1878022
CMKLR1
0.851 0.080 12 108305255 intron variant C/T snv 0.70 1
rs7186128 1.000 0.080 16 16864058 intergenic variant G/A snv 0.70 2
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 2
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 6
rs3110697
IGFBP3
0.827 0.160 7 45915430 intron variant A/G snv 0.58 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs3769821
CASP8
0.851 0.200 2 201258707 intron variant C/T snv 0.57 2
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 1
rs5879422
DCBLD1
1.000 0.080 6 117463495 intron variant -/GT delins 0.54 1
rs11622887
SYNE3
1.000 0.080 14 95476110 upstream gene variant A/C snv 0.52 2
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
rs56113850
CYP2A6
0.807 0.080 19 40847202 intron variant T/C snv 0.52 8
rs753955
LOC105370113
0.776 0.120 13 23719720 regulatory region variant A/G snv 0.50 1
rs2395655
CDKN1A ; DINOL
0.882 0.120 6 36677919 5 prime UTR variant A/G snv 0.43 0.49 2
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 11
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 4
rs4488809
TP63
0.827 0.080 3 189638472 intron variant T/C snv 0.45 1
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 1