Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35530071 17 7659807 downstream gene variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTTT delins 1
rs34717272
RGS2
1 192810962 intron variant TC/CT mnv 1
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 92
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 36
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 24
rs11077
POLR1C ; XPO5
0.732 0.320 6 43523209 3 prime UTR variant T/G snv 0.47 14
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 7
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 6
rs753152
RAMP2-AS1 ; RAMP2
0.882 0.160 17 42761487 intron variant T/G snv 0.12 6
rs805304
CLIC1 ; DDAH2
0.851 0.240 6 31730311 5 prime UTR variant T/G snv 0.48 5
rs2304456
KNG1
0.925 0.120 3 186727263 missense variant T/G snv 0.12 9.3E-02 3
rs26802
GHRLOS ; GHRL
0.925 0.160 3 10290681 intron variant T/G snv 0.31 3
rs45547640
XDH
0.925 0.040 2 31346794 missense variant T/G snv 2.0E-03 6.5E-04 3
rs864265 0.925 0.080 3 186836503 intergenic variant T/G snv 0.86 3
rs569550
LSP1
0.925 0.080 11 1865838 intron variant T/G snv 0.35 2
rs10491093 17 10978681 intergenic variant T/G snv 0.72 1
rs111253292
CORIN
4 47661743 missense variant T/G snv 4.6E-03 2.0E-02 1
rs4496877 7 150983418 intergenic variant T/G snv 0.74 1
rs6749447
STK39
2 168184876 intron variant T/G snv 0.37 1
rs7256241
MIR518C ; LOC107985346
19 53708649 upstream gene variant T/G snv 0.46 1
rs761579841
GRK4
4 3035444 missense variant T/G snv 1
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24