Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10895068
PGR ; PGR-AS1
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs104893831
VHL
0.925 0.040 3 10146549 missense variant G/A;C;T snv 2.0E-05 2
rs2228611
DNMT1
0.708 0.520 19 10156401 synonymous variant T/A;C snv 0.52 19
rs10860812
DRAM1
12 101894592 intron variant G/A snv 0.59 1
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 5
rs6219
HELLPAR ; LINC02456 ; IGF1
1.000 0.080 12 102396414 3 prime UTR variant C/T snv 8.9E-02 2
rs7136446
IGF1 ; LINC02456
0.882 0.160 12 102444737 intron variant C/T snv 0.66 8
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs11568818
MMP7
0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs176185
WBP1L
10 102796297 intron variant G/C snv 0.82 1
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs104894145
CYP17A1-AS1 ; CYP17A1 ; WBP1L
0.925 0.240 10 102830946 missense variant G/A snv 3
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 6
rs4919687
CYP17A1
0.742 0.160 10 102835491 non coding transcript exon variant G/A snv 0.25 6
rs138009835
CYP17A1 ; LOC107984264
10 102839238 intron variant G/A;T snv 1
rs13175330
PAM
5 102840757 intron variant A/G snv 7.8E-02 1
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 97
rs223331
CISD2
0.851 0.160 4 102872408 intron variant T/A;C snv 5
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 30
rs34911341
GHRL ; GHRLOS
0.882 0.200 3 10289835 missense variant C/T snv 7.0E-03 7.3E-03 4
rs26802
GHRLOS ; GHRL
0.925 0.160 3 10290681 intron variant T/G snv 0.31 3