Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs4919686
WBP1L ; CYP17A1 ; CYP17A1-AS1
0.851 0.200 10 102832492 3 prime UTR variant A/C snv 0.23 0.21 4
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs4919687
CYP17A1
0.742 0.160 10 102835491 non coding transcript exon variant G/A snv 0.25 14
rs10786712
CYP17A1
1.000 0.040 10 102836639 intron variant C/T snv 0.38 1
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs11191416
LOC107984264
1.000 0.040 10 102845159 intron variant T/G snv 0.10 1
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 99
rs3093030
ICAM4 ; ICAM1
0.925 0.120 19 10286727 non coding transcript exon variant C/T snv 0.34 6
rs3740390
AS3MT ; BORCS7-ASMT
0.925 0.080 10 102878723 intron variant C/T snv 9.2E-02 2
rs11191447
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102892566 intron variant C/T snv 9.2E-02 1
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs10903323
MSRA
0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs12788925 1.000 0.040 11 102931118 intergenic variant A/G snv 0.32 1
rs12414777
CNNM2
1.000 0.040 10 102938024 intron variant C/G;T snv 0.20 1
rs640198
MMP13
0.851 0.040 11 102954362 intron variant T/G snv 0.68 4
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs10861032
C12orf42
0.925 0.040 12 103518728 non coding transcript exon variant T/C snv 0.24 2
rs9804922
C12orf42
1.000 0.040 12 103519664 intron variant C/T snv 9.5E-02 1
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 6
rs2128739 0.925 0.080 11 103802549 intron variant A/C snv 0.68 2
rs2839812 1.000 0.040 11 103802566 intron variant T/A;C snv 1