Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs1555454508
SPG11
0.790 0.240 15 44615487 stop gained GTA/ATC mnv 18
rs312262717
SPG11
0.790 0.240 15 44659104 frameshift variant A/-;AA delins 18
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 13
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 9
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 9
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 8
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs1057518913
EHMT1
0.851 0.320 9 137762822 splice donor variant T/C snv 7
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 7
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 6
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs389883
CYP21A2 ; STK19
0.827 0.200 6 31979683 non coding transcript exon variant G/T snv 0.80 6
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 6
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 5