Source: BEFREE

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 5
rs1269252748
VLDLR-AS1 ; VLDLR
9 2641436 missense variant C/T snv 4
rs760361706
PPARA
22 46235326 missense variant G/C snv 4.0E-06 4
rs9983925
ADARB1
21 45216929 intron variant C/T snv 0.46 4
rs876660427
APC
5 112838608 missense variant C/T snv 4
rs140516819
EGFR
7 55172999 missense variant A/C;G snv 4.0E-05 2.4E-04 4
rs35918369
EGFR
7 55205613 missense variant C/T snv 3.1E-04 3.3E-04 4
rs1018379423
EPHB2
1 22907986 missense variant G/T snv 4.0E-06 2.1E-05 4
rs767136747
SARDH
9 133717404 missense variant T/C snv 4.0E-06 4
rs1441008398
APC
5 112839334 missense variant C/T snv 4.0E-06 4
rs750605522
GOT2
16 58722168 missense variant T/A snv 4.0E-06 7.0E-06 4
rs863224683
TP53
17 7675224 missense variant G/A;C snv 4
rs1057518011
TMEM240
1 1535766 missense variant C/T snv 4
rs2640909
PER3
1 7830057 missense variant T/C snv 0.14 0.23 4
rs1052108705
TCF19 ; POU5F1
6 31165217 missense variant C/T snv 4.1E-06 2.1E-05 3
rs768746587
TCF19 ; POU5F1
6 31165136 missense variant C/T snv 8.4E-06 3
rs755683317
TPTE
21 10567746 missense variant G/A;C snv 2.4E-05 3
rs778826879
MAPK3
16 30121948 missense variant C/G;T snv 1.2E-05; 8.0E-06 3
rs10505476
PCAT1 ; POU5F1B ; CASC8
8 127395871 intron variant C/T snv 0.38 3
rs770684782
SETX
9 132288268 stop gained G/A snv 4.0E-06 3
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 3
rs1802710
DLK1
14 100734308 synonymous variant T/A;C snv 0.63 3
rs138105638
CYP3A4
7 99766440 stop gained G/A;T snv 6.4E-05 7.7E-05 3
rs11121704
MTOR
1 11233902 intron variant C/A;T snv 3
rs375526265
APEX1
14 20457260 missense variant C/T snv 1.2E-05 2.8E-05 3