Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2754511
BIRC6
0.882 0.040 2 32545090 intron variant A/T snv 0.24 3
rs5745718
HGF
0.882 0.040 7 81718232 intron variant T/G snv 0.82 3
rs11669977
NTF4
0.882 0.040 19 49060867 non coding transcript exon variant A/G snv 0.17 3
rs61732310
NTF4
0.882 0.040 19 49061735 missense variant G/A snv 4.5E-03 2.3E-03 3
rs11720822
PDIA5
0.882 0.040 3 123150194 intron variant C/T snv 8.6E-02 6.6E-02 3
rs2156323
VAV2
0.882 0.040 9 133855699 intron variant G/A snv 9.2E-02 3
rs1466441587
VAV3
0.882 0.040 1 107874935 missense variant G/A snv 7.0E-06 3
rs2801219
VAV3
0.882 0.040 1 107959790 intron variant C/A snv 0.62 3
rs576499843
VAV3
0.882 0.040 1 107617607 missense variant A/C;G snv 8.0E-06 7.0E-06 3
rs1132776
ABCC5
0.925 0.040 3 183978614 synonymous variant A/G snv 0.58 0.61 2
rs939336
ABCC5
0.925 0.040 3 183967746 stop gained A/G;T snv 0.58 2
rs1258267
C10orf53
0.925 0.040 10 49687724 intron variant G/A snv 0.95 2
rs1157699
CALCRL ; LOC105373786
0.925 0.040 2 187394177 intron variant C/G;T snv 2
rs12138977
COL11A1
0.925 0.040 1 102927901 intron variant C/T snv 0.52 2
rs3739821
DPM2 ; FAM102A
0.925 0.040 9 127940198 non coding transcript exon variant A/G snv 0.61 2
rs3816415
EPDR1 ; SFRP4
0.925 0.040 7 37948709 intron variant G/A snv 0.12 2
rs7494379
FERMT2
0.925 0.040 14 52944673 intron variant C/G;T snv 2
rs736893
GLIS3
0.925 0.040 9 4217028 intron variant G/A;C snv 2
rs12540393
HGF
0.925 0.040 7 81734871 intron variant C/T snv 0.77 2
rs17427817
HGF
0.925 0.040 7 81735119 intron variant C/A;G;T snv 2
rs12493550
HTR3D
0.925 0.040 3 184034985 intron variant G/A snv 6.3E-02 2
rs6759535
LOC105373786 ; CALCRL
0.925 0.040 2 187373374 intron variant T/C snv 0.52 2
rs840617
LOC105373786 ; CALCRL
0.925 0.040 2 187365606 intron variant A/T snv 0.80 2
rs1676484
LOC107985096
0.925 0.040 1 102839465 intron variant A/C snv 2
rs756459094
MMP1 ; WTAPP1
0.925 0.040 11 102795237 missense variant T/A;C;G snv 1.6E-05; 4.0E-06 2