Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3732379
CX3CR1
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 10
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 9
rs11915606
BTD
0.925 0.040 3 15633655 intron variant T/G snv 3.4E-02 2
rs138741635
FHIT
0.925 0.040 3 60942161 intron variant T/A;G snv 2
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs144610116
FAM114A1
0.925 0.040 4 38941227 intron variant T/C snv 8.6E-03 2
rs148121703
GABRB1
0.925 0.040 4 47371654 intron variant TGT/- delins 2.6E-03 2
rs192427471 0.925 0.040 4 124644124 intergenic variant C/T snv 2.4E-03 2
rs61361928
UGT2B7
1.000 0.040 4 69096657 missense variant T/C snv 2.6E-03 2.8E-03 1
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs201394051 0.925 0.040 5 117697919 intergenic variant TA/-;TATA;TATATA delins 2
rs1235324522
F2R
1.000 0.040 5 76732662 missense variant C/T snv 4.0E-06 1.4E-05 1
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs76863441
PLA2G7
0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs6922269
MTHFD1L
0.807 0.200 6 150931849 intron variant G/A snv 0.35 7
rs186696265 0.882 0.040 6 160690668 intergenic variant C/T snv 1.0E-02 6
rs181937009
LOC107986652 ; LOC100507477
0.925 0.040 6 140064258 intron variant A/G snv 0.23 3
rs149232047 0.925 0.040 6 126276990 intergenic variant A/G snv 1.5E-04 2
rs3087459
EDN1
0.925 0.160 6 12289406 upstream gene variant A/C snv 0.20 2
rs4357117
LOC107986540
0.925 0.040 6 66873865 intergenic variant G/T snv 1.7E-02 2
rs9295128 0.925 0.040 6 160330499 intergenic variant G/T snv 1.1E-02 2