Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4656461 0.827 0.040 1 165717968 TF binding site variant G/A snv 0.85 7
rs1015213 0.851 0.040 8 51974981 intron variant C/T snv 0.14 6
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
rs2754511
BIRC6
0.882 0.040 2 32545090 intron variant A/T snv 0.24 3
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
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs1676486
COL11A1
0.851 0.120 1 102888582 missense variant A/G;T snv 0.80; 4.0E-06 7
rs3753841
COL11A1
0.827 0.080 1 102914362 missense variant G/A snv 0.61 0.49 7
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
rs3735520
HGF
0.851 0.040 7 81771623 upstream gene variant G/A;T snv 4
rs5745718
HGF
0.882 0.040 7 81718232 intron variant T/G snv 0.82 3
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
rs1043618
HSPA1L ; HSPA1A
0.752 0.280 6 31815730 5 prime UTR variant G/A;C;T snv 0.39; 2.0E-05; 4.0E-06 10
rs12493550
HTR3D
0.925 0.040 3 184034985 intron variant G/A snv 6.3E-02 2
rs1900004
LINC02640
0.827 0.040 10 68241124 intron variant C/T snv 0.39 5
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