Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 47
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 45
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 42
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 40
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 38
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 36
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 36
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 35
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 35
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33