Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9610915
MAFF
1.000 0.080 22 38215073 3 prime UTR variant C/G snv 0.48 0.41 1
rs918140013
ATXN2 ; SH2B3
0.925 0.080 12 111447663 missense variant G/A snv 7.0E-06 2
rs886063722
AGPAT2
1.000 0.080 9 136677118 missense variant G/A snv 4.0E-06 1
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs799917
BRCA1
0.708 0.320 17 43092919 missense variant G/A;C;T snv 0.40; 1.6E-05 18
rs796065343
CSF3R
0.776 0.080 1 36467833 missense variant G/A snv 12
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs775014154
RSPH14 ; BCR
1.000 0.080 22 23181637 missense variant C/T snv 5.8E-05 7.0E-05 1
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs768288452
BCR ; RSPH14
1.000 0.080 22 23181822 missense variant A/G snv 4.1E-06 1
rs766124888
BCR
1.000 0.080 22 23253817 missense variant C/A;G snv 4.0E-06; 4.0E-06 1
rs762613037
SLC19A1 ; COL18A1
0.790 0.160 21 45512196 missense variant A/G snv 2.1E-05 7.0E-06 7
rs760454379
IKZF1
1.000 0.080 7 50400082 missense variant G/A snv 1.6E-05 7.0E-06 1
rs755796482
ATXN2 ; SH2B3
1.000 0.080 12 111447512 missense variant G/A snv 4.1E-06 8.1E-06 1
rs754736070
MTTP
1.000 0.080 4 99597206 missense variant T/C snv 8.0E-06 7.0E-06 1
rs754541813
FLNB
1.000 0.080 3 58123401 synonymous variant C/T snv 6.8E-05 2.8E-05 1
rs748843032
MTTP
0.807 0.160 4 99594840 missense variant T/C snv 4.0E-06 8
rs717620
ABCC2
0.763 0.240 10 99782821 5 prime UTR variant C/T snv 0.17 0.15 10
rs6931104
ARMT1
1.000 0.080 6 151465042 intron variant G/A snv 0.54 1
rs683369
SLC22A1
0.807 0.360 6 160130172 missense variant G/A;C;T snv 4.0E-06; 0.83; 4.0E-06 7
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs6503691
STAT5B
0.827 0.200 17 42242072 intron variant C/T snv 0.26 5
rs636832
AGO1
0.790 0.400 1 35897874 intron variant G/A snv 0.23 8
rs628031
SLC22A1
0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 8