Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6590811
ARHGAP42
11 100708153 intron variant C/T snv 0.53 4
rs6590812
ARHGAP42
11 100711497 intron variant G/A snv 0.55 1
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs6590816
ARHGAP42
11 100730902 intron variant G/A snv 0.40 4
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs7801190
SLC12A9
1.000 0.040 7 100860471 non coding transcript exon variant C/G snv 9.9E-02 2
rs104893831
VHL
0.925 0.040 3 10146549 missense variant G/A;C;T snv 2.0E-05 2
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs11568818
MMP7
0.763 0.280 11 102530930 upstream gene variant T/A;C snv 2
rs104894145
CYP17A1-AS1 ; CYP17A1 ; WBP1L
0.925 0.240 10 102830946 missense variant G/A snv 1
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 8
rs4919687
CYP17A1
0.742 0.160 10 102835491 non coding transcript exon variant G/A snv 0.25 9
rs13175330
PAM
5 102840757 intron variant A/G snv 7.8E-02 1
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs4409766
BORCS7-ASMT ; BORCS7
1.000 0.040 10 102856906 intron variant T/C snv 0.14 6
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 2
rs34911341
GHRL ; GHRLOS
0.882 0.200 3 10289835 missense variant C/T snv 7.0E-03 7.3E-03 2
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 6
rs11191514
CNNM2
10 103013607 intron variant C/G;T snv 1
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 7
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs12219304
NT5C2
10 103171827 intron variant G/C;T snv 1
rs11191593
NT5C2
10 103179458 intron variant T/C snv 9.0E-02 4
rs112913898 10 103199143 intergenic variant G/A snv 9.1E-02 3
rs4387287
STN1
10 103918139 5 prime UTR variant A/C snv 0.69 3