Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9282861
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 31
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs13387042
LOC105373874 ; LOC101928278
0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 16
rs72661131
MBL2
0.742 0.480 10 52771739 upstream gene variant A/G snv 7.6E-04 15
rs10895068
PGR ; PGR-AS1
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs34598529
HBB
0.724 0.280 11 5227100 5 prime UTR variant T/C snv 8.9E-04 14
rs562962093
MBL2
0.742 0.520 10 52771740 upstream gene variant T/C snv 7.0E-06 13
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 11
rs63750953
HBB
0.790 0.400 11 5227097 5 prime UTR variant TT/- delins 7.0E-06 10
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53 8
rs999737
RAD51B
0.776 0.200 14 68567965 intron variant C/T snv 0.16 8
rs6504950
STXBP4
0.807 0.120 17 54979110 intron variant G/A snv 0.29 7
rs1314913
RAD51B
0.807 0.120 14 68232877 intron variant C/T snv 0.13 6
rs137852573
AR
0.807 0.280 X 67686064 missense variant G/A snv 6
rs2588809
RAD51B
0.807 0.160 14 68193711 intron variant T/C snv 0.80 6
rs33931746
HBB
0.807 0.280 11 5227099 5 prime UTR variant T/C;G snv 6
rs34166473
HBD
0.827 0.320 11 5234513 5 prime UTR variant A/G snv 7.0E-06 6
rs35518301
HBD
0.827 0.200 11 5234514 5 prime UTR variant T/C snv 6
rs137852576
AR
0.827 0.240 X 67686067 missense variant G/A snv 5
rs183433761
GCG ; LOC101929532
0.851 0.200 2 162152278 5 prime UTR variant T/C;G snv 5
rs200487063
LEP
0.851 0.200 7 128241246 upstream gene variant G/A snv 2.1E-05 5
rs33980857
HBB
0.827 0.280 11 5227101 5 prime UTR variant A/C;G;T snv 5
rs33981098
HBB
0.827 0.280 11 5227102 5 prime UTR variant T/C;G snv 5