Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12040333
ST3GAL3
1.000 0.080 1 43848369 intron variant G/A;C snv 2
rs12051548
TM4SF5
17 4779740 intron variant G/C snv 7.5E-02 1
rs12507628 4 72779634 regulatory region variant G/A snv 0.13 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10
rs1303
SERPINA1
0.925 0.040 14 94378506 missense variant T/G snv 0.28 0.22 4
rs13175840 1.000 0.080 5 133861647 regulatory region variant A/G snv 0.25 2
rs1333036
CDKN2B-AS1
1.000 0.040 9 22043820 intron variant T/C snv 0.58 2
rs1333037
CDKN2B-AS1
0.925 0.040 9 22040766 intron variant C/T snv 0.71 3
rs1333039
CDKN2B-AS1
1.000 0.040 9 22065658 splice region variant G/A;C;T snv 2
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 7
rs1333043
CDKN2B-AS1
9 22106732 intron variant T/A snv 0.64 2
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs1333046
CDKN2B-AS1
0.925 0.080 9 22124124 intron variant T/A snv 0.43 4
rs1333047
CDKN2B-AS1
0.790 0.240 9 22124505 intron variant A/T snv 0.63 9
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1333050
CDKN2B-AS1
9 22125914 intron variant C/T snv 0.50 1
rs1360589
CDKN2B-AS1
1.000 0.040 9 22045318 intron variant C/T snv 0.72 2
rs1360590
CDKN2B-AS1
1.000 0.040 9 22041444 intron variant T/C;G snv 2
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs1412834
CDKN2B-AS1
0.790 0.080 9 22110132 intron variant T/C snv 0.64 11
rs1440581
PPM1K-DT
1.000 0.080 4 88305270 intron variant T/A;C snv 4
rs1481805 1.000 0.080 8 71121190 intron variant A/T snv 0.58 2