Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28933068
FGFR3
0.645 0.560 4 1805644 missense variant C/A;G;T snv 1.6E-05 30
rs104893951
FOXC1
0.851 0.080 6 1610780 missense variant T/A;C snv 8.0E-06 5
rs121918214
FTO
1.000 0.200 16 53873837 missense variant G/A snv 4.0E-06 7.0E-06 3
rs745616565
FTO
1.000 0.200 16 53873855 missense variant G/A snv 1.6E-05 2.1E-05 3
rs781028867
FTO
1.000 0.200 16 53873846 missense variant C/A;T snv 4.0E-06 3
rs397514698
GNAQ
0.667 0.400 9 77797577 missense variant C/T snv 52
rs757956956
GPI
19 34377533 missense variant A/G snv 4.0E-06 1
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs121909173
HESX1
0.851 0.240 3 57199901 missense variant C/G snv 2.8E-05 1.4E-05 5
rs104894232
HYLS1 ; PUS3
0.925 0.160 11 125900000 missense variant A/G snv 1.1E-03 1.0E-03 4
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs587777570
KIF5C
1.000 2 148947018 missense variant G/A snv 4
rs756632799
LOC107985405 ; PIGT
0.882 0.080 20 45416579 stop gained G/T snv 1.6E-05 7.0E-06 5
rs121918355
LTBP2
0.807 0.280 14 74555629 stop gained G/A;T snv 2.1E-05; 4.2E-06 7
rs4954218
MAP3K19
0.925 0.080 2 135045855 intron variant G/T snv 0.83 5
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs368705607
MIXL1
0.882 0.120 1 226225766 missense variant T/C;G snv 2.8E-05; 4.0E-06 7
rs121909497
MMP13
0.925 0.080 11 102955390 missense variant A/G snv 3
rs2236225
MTHFD1
0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
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
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1387329667
NOTCH1
9 136500595 missense variant G/A snv 2