Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137854438
FAM83H
1.000 0.080 8 143728570 stop gained A/T snv 2
rs1387329667
NOTCH1
9 136500595 missense variant G/A snv 2
rs142322800
FCGR3A
1 161548502 missense variant T/C snv 1.5E-04 5.6E-05 1
rs1554442016
TWIST1
0.882 0.080 7 19116972 missense variant T/A;C snv 4
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1801198
TCN2
0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs201405525
DECR1
0.925 0.240 8 90044993 missense variant G/A;C snv 4.5E-04; 4.0E-06 3
rs201968272
DDX11
0.925 0.160 12 31089147 missense variant G/A snv 3
rs2236225
MTHFD1
0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs28933068
FGFR3
0.645 0.560 4 1805644 missense variant C/A;G;T snv 1.6E-05 30
rs28939086
SLC26A4
0.925 0.160 7 107690220 missense variant A/C;G snv 2.0E-04; 4.0E-06 4
rs368087026
SLC19A1
0.637 0.520 21 45530890 missense variant G/A snv 33
rs368705607
MIXL1
0.882 0.120 1 226225766 missense variant T/C;G snv 2.8E-05; 4.0E-06 7
rs387906617
CREB1
2 207567506 missense variant A/G snv 2
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs397514606
AKT3
0.763 0.320 1 243695714 missense variant C/T snv 14
rs397514698
GNAQ
0.667 0.400 9 77797577 missense variant C/T snv 52
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
rs504849
WNT5A
3 55488911 intron variant T/C;G snv 1
rs524153
WNT5A
3 55491957 upstream gene variant T/A;G snv 1
rs527236031
PIGT ; MIR6812
0.882 0.080 20 45424323 missense variant C/T snv 1.6E-05 4.2E-05 5