Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs945006
DIO3
1.000 0.040 14 101562940 3 prime UTR variant T/G snv 0.20 1
rs2287047
IL1R1
1.000 0.040 2 102157594 intron variant G/A snv 0.39 1
rs778767225
MOK
0.851 0.200 14 102231805 missense variant C/A snv 2.4E-05 7.0E-06 4
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1254566330
MOK
0.925 0.120 14 102250845 stop gained C/T snv 7.0E-06 2
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1940475
MMP8
1.000 0.040 11 102722517 missense variant T/C;G snv 0.54 4
rs513964
MMP1 ; WTAPP1
1.000 0.040 11 102795478 missense variant T/C snv 1.9E-04 7.7E-04 1
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs639752
WTAPP1 ; MMP3
0.882 0.120 11 102836608 non coding transcript exon variant C/A snv 0.54 3
rs650108
MMP3
0.827 0.160 11 102838056 intron variant G/A snv 0.31 6
rs520540
MMP3
0.925 0.120 11 102838694 synonymous variant A/G snv 0.57 0.54 2
rs602128
MMP3
1.000 0.040 11 102842734 missense variant A/C;G snv 4.0E-06; 0.57 1
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs1676486
COL11A1
0.851 0.120 1 102888582 missense variant A/G;T snv 0.80; 4.0E-06 7
rs2615977
COL11A1
0.925 0.080 1 102986836 intron variant A/C snv 0.27 3
rs2622873
COL11A1
0.882 0.040 1 103000497 intron variant T/C;G snv 3
rs4907986
COL11A1
0.925 0.040 1 103084077 intron variant C/T snv 0.49 2
rs835487
CHST11
0.925 0.040 12 104666989 intron variant A/G snv 0.43 2
rs1560707
SLC44A2
1.000 0.040 19 10640062 intron variant T/A;G snv 1
rs3815148
COG5
1.000 0.040 7 107297975 intron variant A/C snv 0.20 1
rs4730250
DUS4L
1.000 0.040 7 107567250 intron variant A/G snv 0.12 1
rs2966417
LOC105375451
1.000 0.040 7 110517489 intron variant A/G snv 0.69 1
rs10980705
LPAR1
1.000 0.040 9 111040905 upstream gene variant C/T snv 0.18 1
rs1034528
MTOR ; ANGPTL7
0.882 0.120 1 11189075 intron variant G/C snv 0.30 5