Disease: Diabetes
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1073203 0.882 0.160 5 125983763 intron variant C/G snv 0.15 4
rs11196205
TCF7L2
0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs1241356540
ACE
0.851 0.160 17 63497137 missense variant C/T snv 5
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs3134069
COLEC10 ; TNFRSF11B
0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4838605
ARHGAP22
0.882 0.160 10 48491914 intron variant C/T snv 0.38 4
rs659366
UCP2
0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs9640883
LOC105375519
0.882 0.120 7 134431881 intron variant G/A snv 0.21 4
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
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
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
rs713041
GPX4
0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48