Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs228648
UTS2
0.776 0.360 1 7853370 missense variant G/A snv 0.51 0.52 13
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 9
rs1057519914
MTOR
0.851 0.240 1 11157174 missense variant A/G snv 5
rs1057519915
MTOR
0.851 0.160 1 11109318 missense variant A/C snv 5
rs753535070
MUC1
0.851 0.120 1 155187350 missense variant T/C snv 8.0E-06 5
rs1057519916
MTOR
0.882 0.160 1 11109320 missense variant T/A snv 4
rs786205165
MTOR
0.882 0.120 1 11157173 missense variant C/A;T snv 4
rs1057519913
MTOR
0.925 0.120 1 11157172 missense variant G/C snv 3
rs35490896
CLSPN
0.925 0.080 1 35736984 missense variant G/A snv 5.5E-02 6.5E-02 3
rs1704754
HSD17B7
1 162790761 5 prime UTR variant C/T snv 0.70 0.62 1
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs1057520009
XPO1
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs113994087
ALK
0.827 0.120 2 29209798 missense variant C/A;T snv 12
rs28997576
BARD1
0.776 0.160 2 214752454 missense variant C/G;T snv 1.5E-02 11
rs63750624
MSH2
0.925 0.160 2 47410211 missense variant G/A snv 6
rs1057520010
XPO1
0.882 0.200 2 61492336 missense variant T/A;G snv 5
rs754688962
SF3B1
0.851 0.200 2 197402637 missense variant T/C;G snv 5
rs11895168
ERBB4
0.925 0.080 2 211377467 3 prime UTR variant A/C snv 0.68 4
rs1972820
ERBB4
0.925 0.080 2 211378697 3 prime UTR variant G/A snv 0.63 3
rs1553622530
BARD1
2 214781220 stop gained C/T snv 1
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71