Disease: Diabetes
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1298417395
COP1
0.882 0.080 1 176206716 missense variant C/T snv 1.4E-05 4
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs3861950
TNFSF4
0.827 0.160 1 173187153 intron variant T/C snv 0.47 7
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4076317
ANGPTL4
0.882 0.080 19 8364115 intron variant C/G snv 0.25 5
rs4821480
MYH9
0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs4862423
ACSL1
0.882 0.080 4 184805394 intron variant C/T snv 0.37 4
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs774887459
SGSM3
0.882 0.080 22 40405776 missense variant G/A snv 4.0E-06 4
rs1440763451
PPARG
0.882 0.080 3 12416849 missense variant A/G snv 4.0E-06 4
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs16139
NPY ; LOC107986777
0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs773297988
PIK3CB
0.882 0.080 3 138698965 missense variant T/C snv 4.0E-06 3.5E-05 4