Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs867114783
TP53
17 7675109 missense variant T/C snv 6
rs1018379423
EPHB2
1 22907986 missense variant G/T snv 4.0E-06 2.1E-05 4
rs140516819
EGFR
7 55172999 missense variant A/C;G snv 4.0E-05 2.4E-04 4
rs1441008398
APC
5 112839334 missense variant C/T snv 4.0E-06 4
rs3136558
IL1B
1.000 2 112833698 intron variant A/G snv 0.21 4
rs35918369
EGFR
7 55205613 missense variant C/T snv 3.1E-04 3.3E-04 4
rs750605522
GOT2
16 58722168 missense variant T/A snv 4.0E-06 7.0E-06 4
rs7668666
TLR3
1.000 4 186080138 intron variant C/A;T snv 4
rs767136747
SARDH
9 133717404 missense variant T/C snv 4.0E-06 4
rs876660427
APC
5 112838608 missense variant C/T snv 4
rs10505476
PCAT1 ; POU5F1B ; CASC8
8 127395871 intron variant C/T snv 0.38 3
rs1056663
HUS1
1.000 7 47965365 synonymous variant C/T snv 0.49 0.46 3
rs11121704
MTOR
1 11233902 intron variant C/A;T snv 3
rs1372047743
MCM4 ; PRKDC
8 47960120 missense variant C/T snv 9.7E-06 3
rs138105638
CYP3A4
7 99766440 stop gained G/A;T snv 6.4E-05 7.7E-05 3
rs151227402
SLC2A9 ; DRD5
4 9783126 missense variant A/G snv 8.0E-05 3.1E-04 3
rs1639122
CHD4
12 6601981 missense variant C/A;G snv 0.40 3
rs16861205
ADIPOQ
3 186843845 intron variant G/A snv 0.14 3
rs1800932
MSH6 ; FBXO11
2 47790942 synonymous variant A/G snv 0.13 0.15 3
rs2071214
BIRC5
17 78223510 missense variant G/A snv 0.93 0.96 3
rs2294757
VNN1
6 132713959 missense variant G/A snv 0.45 0.53 3
rs267606704
CBL
1.000 11 119278170 missense variant A/C;G snv 3
rs2970870
PPARGC1A
4 23891394 intron variant A/G snv 0.49 3
rs3087465
TGFBR2 ; LOC105377015
1.000 3 30605668 upstream gene variant A/G;T snv 0.64 3
rs3087468
NTHL1
16 2040233 missense variant C/A snv 3