Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1060743
BIN1
0.925 0.080 2 127068957 synonymous variant A/G snv 0.34 0.29 2
rs35349669
INPP5D
0.925 0.080 2 233159830 intron variant C/T snv 0.35 2
rs10197851
HPCAL1
1.000 0.080 2 10345283 intron variant A/G snv 0.52 1
rs138047593
BIN1
1.000 0.080 2 127050470 missense variant T/C snv 9.2E-03 8.2E-03 1
rs4669573
HPCAL1
1.000 0.080 2 10338810 intron variant A/G snv 0.47 1
rs67327804
BIN1
1.000 0.080 2 127069056 intron variant A/G snv 0.30 0.33 1
rs754834233
BIN1
1.000 0.080 2 127059060 missense variant G/A snv 4.1E-05 1
rs775494528
BIN1
1.000 0.080 2 127057558 missense variant G/A snv 7.0E-06 1
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs3732379
CX3CR1
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs2304456
KNG1
0.925 0.120 3 186727263 missense variant T/G snv 0.12 9.3E-02 4
rs710446
KNG1
0.925 0.120 3 186742138 missense variant T/C snv 0.42 0.44 4
rs6784615
NISCH
1.000 0.080 3 52472410 intron variant C/T snv 0.96 0.96 2
rs11711889
LINC02006
1.000 0.080 3 153652877 intron variant G/A snv 0.12 1
rs6665
MME
1.000 0.080 3 155183416 3 prime UTR variant C/A;G snv 1
rs137875858
UNC5C
0.925 0.080 4 95170280 missense variant G/A snv 2.9E-04 2.6E-04 2
rs17070145
WWC1
0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs3730089
PIK3R1
0.827 0.280 5 68292320 missense variant G/A snv 0.18 0.22 5
rs190982
MEF2C-AS1
0.925 0.080 5 88927603 intron variant G/A snv 0.72 2