Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs769217
CAT
0.742 0.440 11 34461361 synonymous variant C/T snv 0.25 0.22 12
rs35677492
CAT
0.925 0.040 11 34471409 synonymous variant G/A snv 5.0E-04 2.7E-04 2
rs4756146
CAT
0.925 0.080 11 34442192 intron variant T/C snv 0.12 2
rs769214
CAT
0.925 0.160 11 34438170 upstream gene variant G/A snv 0.61 2
rs7943316
CAT
0.925 0.040 11 34438925 upstream gene variant A/T snv 0.57 2
rs1212131663
CAT
1.000 0.080 11 34439050 stop gained C/T snv 7.0E-06 1
rs1402522059
CAT
1.000 0.080 11 34449312 missense variant C/G;T snv 4.0E-06 1
rs1428168076
CAT
1.000 0.120 11 34452152 missense variant A/C snv 8.0E-06 7.0E-06 1
rs2284367
CAT
11 34462995 intron variant T/C snv 0.22 1
rs511895
CAT
1.000 0.160 11 34466182 intron variant T/C snv 0.70 1
rs7933285
CAT
11 34455578 intron variant C/T snv 0.22 1
rs7947841
CAT
11 34470133 intron variant G/A snv 1.0E-01 1
rs564250
LOC105376622 ; CAT
1.000 0.080 11 34437314 upstream gene variant T/A;C snv 1