Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2660852 12 96051770 intergenic variant C/A snv 0.34 3
rs35697691
LOC112268150 ; MAPK6
15 52061301 missense variant C/G snv 5.8E-02 5.9E-02 3
rs1156560901
CDK15
2 201880120 missense variant A/G snv 1.4E-05 2
rs181264737
MTSS1
8 124589710 missense variant C/A;G;T snv 1.2E-05; 4.1E-06; 4.1E-06 2
rs1022088103
MMP2
16 55485759 missense variant G/A snv 1
rs1033313160
MAPKAP1
9 125506375 missense variant G/T snv 1
rs1223118092
LOC100506142 ; RHOQ
2 46576601 missense variant A/G snv 1
rs1231584616
MMP2
16 55485367 missense variant G/A snv 4.0E-06 1
rs138281457
GRAP2
22 39955861 missense variant A/G snv 4.0E-06 3.5E-05 1
rs1383618437
ATAT1
6 30627473 missense variant C/A snv 4.0E-06 1
rs1442033697
SERPINE1
7 101135780 frameshift variant A/- del 1
rs1453208391
HGF
7 81707297 missense variant G/A snv 4.0E-06 1
rs367569800
PLXNA1
3 127014358 missense variant G/A;C snv 6.7E-05; 1.0E-04 1
rs367827951
PLAT
8 42182000 missense variant G/A;C snv 4.0E-06; 2.8E-05 1
rs371731991
RET
10 43109220 missense variant G/A;C snv 2.0E-05; 4.0E-06 1
rs3918252
MMP9
20 46010492 missense variant C/G snv 3.6E-05 2.4E-04 1
rs4328905
HPSE
4 83322396 intron variant A/G snv 0.18 0.18 1
rs6737848
SOCS5 ; LINC01118
2 46701027 intron variant C/G snv 0.14 1
rs757786591
WNT10A
2 218890134 missense variant G/A snv 4.4E-05 2.1E-05 1
rs757816355
KRAS
12 25225657 missense variant C/T snv 1.2E-05 7.0E-06 1
rs763116801
TP63
3 189869342 missense variant A/C;G snv 4.0E-06; 8.0E-06 1
rs765715998
HCK
20 32083944 missense variant G/A snv 2.4E-05 2.1E-05 1
rs770795658
PGR ; PGR-AS1
11 101127788 missense variant C/T snv 6.1E-06 7.0E-06 1
rs771086543
FBXL15 ; CUEDC2
10 102422814 missense variant G/A snv 1.3E-04 1.0E-04 1
rs771799019
GRAP2
22 39969528 missense variant G/T snv 8.0E-06 7.0E-06 1