Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2302615
ODC1-DT ; SNORA80B ; ODC1
0.807 0.120 2 10448012 intron variant C/T snv 0.31 7
rs1535989 0.925 0.080 13 105370372 intergenic variant A/G;T snv 4
rs17503908
ATM ; C11orf65
1.000 0.080 11 108344670 intron variant T/G snv 6.7E-02 2
rs142287570
GCM2
1.000 6 10874335 missense variant T/G snv 6.6E-04 4.9E-04 2
rs371918069
GCM2
1.000 6 10874372 missense variant C/T snv 5.6E-05 5.6E-05 2
rs61734277
GCM2
0.882 0.080 6 10874672 missense variant A/C snv 9.1E-03 8.6E-03 5
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs1268298845
APC
0.882 0.120 5 112780878 missense variant G/A snv 4.0E-06 4
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 17
rs459552
APC
0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 14
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs7131056
DRD2
0.827 0.200 11 113459052 intron variant A/C snv 0.51 6
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins 11
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs7873784
TLR4
0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 11
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs3842787
PTGS1
0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 11
rs5789
PTGS1
1.000 0.080 9 122381694 missense variant C/A snv 1.8E-02 1.8E-02 2
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10505476
PCAT1 ; POU5F1B ; CASC8
8 127395871 intron variant C/T snv 0.38 3
rs10808555
PCAT1 ; POU5F1B ; CASC8
0.925 0.080 8 127397266 intron variant G/A snv 0.65 6