Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052717
SREBF2
0.925 0.080 22 41885425 intron variant A/G snv 0.62 3
rs1053239
CIDEC
1.000 0.040 3 9867065 3 prime UTR variant G/C snv 0.19; 5.6E-05 0.14 1
rs1055419
OSBPL11
1.000 0.040 3 125594988 5 prime UTR variant G/A snv 7.6E-02 1
rs1057972
IL15
0.790 0.200 4 141733279 3 prime UTR variant A/T snv 0.54 7
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 7
rs10746473
PER3
1.000 0.040 1 7817996 intron variant A/G snv 0.58 1
rs10749127
TCF7L2
1.000 0.040 10 113089594 intron variant C/T snv 0.28 1
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 7
rs10830956 1.000 0.040 11 92947847 intergenic variant C/T snv 0.33 1
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 7
rs10833
IL15
0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs10838681
NR1H3
1.000 0.040 11 47253513 intron variant G/A snv 0.34 3
rs10845640
APOBEC1
1.000 0.040 12 7659861 intron variant C/T snv 0.34 1
rs10849915
CCDC63
0.925 0.080 12 110895818 intron variant T/C snv 0.39 3
rs10850335
TBX5
0.925 0.200 12 114375303 intron variant T/C snv 3.1E-02 2
rs10877887
LINC01465 ; MIRLET7I
0.701 0.440 12 62603400 non coding transcript exon variant T/C snv 0.42 18
rs10892044
SIK3
1.000 0.040 11 116896183 intron variant T/C snv 0.16 1
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs10920533
ADIPOR1
1.000 0.040 1 202956690 intron variant G/A snv 0.22 1
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs11039155
NR1H3
0.827 0.400 11 47259211 5 prime UTR variant G/A snv 0.14 0.12 6
rs11063069
CCND2-AS1
0.925 0.080 12 4265207 intron variant A/G snv 0.20 2
rs11065756
CCDC63
0.925 0.080 12 110900990 intron variant C/T snv 6.1E-02 3
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15