Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34329
CDKN1B
1.000 0.080 12 12720299 intron variant G/C snv 0.61 2
rs3757769
SND1
1.000 0.080 7 127901009 intron variant A/G snv 9.7E-02 2
rs563691424
WNK1
1.000 0.080 12 753860 missense variant C/T snv 6.2E-05 2.1E-05 2
rs587778718
TP53
1.000 0.080 17 7674959 missense variant G/A;C;T snv 4.0E-06; 1.2E-05; 4.0E-06 2
rs7085532
TCF7L2
1.000 0.080 10 113099704 intron variant G/A snv 0.72 2
rs771266873
GORASP1
1.000 0.080 3 39098828 missense variant G/A;C snv 2
rs7778413
SND1
1.000 0.080 7 127717662 intron variant T/C snv 0.23 2
rs8089104
SERPINB5
1.000 0.080 18 63480916 intron variant C/T snv 0.50 2
rs8181047
CDKN2B-AS1
0.807 0.120 9 22064466 intron variant A/G snv 0.79 7
rs13332
CTSB
0.925 0.120 8 11849072 synonymous variant T/C;G snv 3.5E-02; 0.56 6
rs1533767
WNT11
0.851 0.120 11 76194756 splice region variant G/A snv 0.27 0.23 5
rs16932912
RECK
0.882 0.120 9 36087879 missense variant G/A snv 9.2E-02 8.5E-02 5
rs678653
CCND1
0.925 0.120 11 69651969 3 prime UTR variant C/G;T snv 5
rs8898
CTSB
0.925 0.120 8 11845033 3 prime UTR variant T/C snv 0.37 5
rs10900598
MDM4
0.882 0.120 1 204556440 3 prime UTR variant G/C;T snv 0.38 4
rs1406
CCNE1
0.882 0.120 19 29824205 3 prime UTR variant C/A snv 0.28 4
rs2071676
ARHGEF39 ; CA9
0.925 0.120 9 35674056 missense variant G/A snv 0.37 0.30 4
rs281377
FUT2 ; LOC105447645
0.925 0.120 19 48703346 synonymous variant C/T snv 0.49 0.42 4
rs708111 0.882 0.120 1 228003664 upstream gene variant G/A snv 0.48 4
rs9879992
GSK3B
0.882 0.120 3 119993874 intron variant A/G snv 0.28 4
rs2289520
SERPINB5
0.925 0.120 18 63493087 missense variant G/A;C snv 0.14 3
rs511044
CASP5
0.925 0.120 11 105024783 upstream gene variant T/C snv 3
rs72696119
LOC105377621 ; NFKB1
0.925 0.120 4 102501347 5 prime UTR variant C/G snv 0.43 3
rs7834169 0.925 0.120 8 27052774 upstream gene variant C/G snv 0.16 3
rs1271546630
MPO
1.000 0.120 17 58277848 missense variant G/A;C snv 2