Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1179225338
TLR4
0.851 0.120 9 117713505 synonymous variant C/T snv 4.0E-06 4
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs4846048
MTHFR ; C1orf167
0.752 0.280 1 11786195 3 prime UTR variant G/A snv 0.67 10
rs55763075
MTHFR ; C1orf167
0.827 0.120 1 11790377 3 prime UTR variant C/T snv 2.1E-05 6
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs768873896
MTHFR
0.790 0.160 1 11794822 missense variant C/G;T snv 8.0E-06; 2.4E-05 7
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs11064
TNFAIP8
0.807 0.120 5 119393693 3 prime UTR variant A/G snv 0.27 9
rs3826392
ZNF18 ; MAP2K4
0.827 0.200 17 12019587 intron variant G/T snv 0.65 5
rs3809728
MAP2K4 ; ZNF18
0.851 0.120 17 12019847 intron variant A/C;T snv 4
rs929783669
STK11
1.000 0.080 19 1220674 missense variant T/C snv 1
rs1834306
MIR10526 ; MIR100 ; MIR100HG
0.776 0.200 11 122152479 intron variant A/G snv 0.49 9
rs300574
SPRY1
0.882 0.080 4 123402583 3 prime UTR variant T/C snv 0.58 0.54 3
rs10893506
ST3GAL4
0.882 0.080 11 126406065 5 prime UTR variant T/A;C snv 6.4E-06; 0.41 5
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs140693
MBD4
0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 10
rs773919809
MGMT
0.763 0.200 10 129766957 missense variant C/T snv 2.0E-05 13
rs1195571 0.882 0.080 12 130739483 intergenic variant T/C snv 0.97 3
rs402710
CLPTM1L
0.716 0.320 5 1320607 non coding transcript exon variant C/T snv 0.33 0.38 18
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs4636297
EGFL7 ; MIR126
0.724 0.360 9 136670698 intron variant A/G snv 0.67 0.65 14
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46