Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9943582
APLNR
0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs991104525
ARSB
0.882 0.160 5 78969051 missense variant G/A snv 1.2E-05 7.7E-05 4
rs9909004
PRKCA
0.925 0.040 17 66310015 intron variant C/T snv 0.59 2
rs9885413 0.925 0.040 5 110840429 intergenic variant G/T snv 0.19 2
rs9838915
KLF15
0.882 0.120 3 126347377 intron variant G/A snv 0.19 4
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs958546
LRRC63
0.882 0.040 13 46259582 intron variant G/C snv 0.29 3
rs9470398
CPNE5
1.000 0.040 6 36799290 intron variant T/C snv 5.5E-02 3
rs9351814 0.882 0.040 6 71484004 intergenic variant A/C snv 0.35 4
rs9303504
PRKCA
0.925 0.040 17 66319248 intron variant G/C snv 0.59 2
rs911119
CST3
0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs899115126
EDNRA
0.882 0.080 4 147542603 missense variant G/C snv 3
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs8179090
TIMP2
0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 12
rs8105292
LINC01782
1.000 0.040 19 32103916 non coding transcript exon variant T/C snv 0.19 3
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs79661299 1.000 0.040 6 42088268 downstream gene variant C/G;T snv 3
rs7965830
LOC105369844
1.000 0.040 12 75962050 intron variant C/A;T snv 3
rs78314028
CYTH3
1.000 0.040 7 6163445 3 prime UTR variant C/A snv 2.2E-02 3
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18