Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3816873
MTTP
0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 9
rs1430583
UCP1
4 140565830 intron variant C/T snv 0.20 1
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1211098985
MTRR
1.000 0.040 5 7878128 missense variant T/C;G snv 4.0E-06 3
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs2016520
PPARD
0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs6929846
BTN2A1
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70 10
rs763000109
TNF
0.827 0.240 6 31575788 missense variant C/G;T snv 4.1E-06; 1.6E-05 9
rs6922269
MTHFD1L
0.807 0.200 6 150931849 intron variant G/A snv 0.35 7
rs9370867
MYLIP
0.827 0.120 6 16145094 missense variant A/G snv 0.60 0.63 7
rs805297
BAG6 ; APOM
0.851 0.280 6 31654829 intron variant C/A snv 0.23 6
rs11961407
CCHCR1
6 31154630 missense variant G/A snv 3.0E-03 1.3E-02 2
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs16139
NPY ; LOC107986777
0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs3812316
MLXIPL
0.763 0.240 7 73606007 missense variant C/G snv 0.10 9.4E-02 14
rs1984112
CD36
0.807 0.280 7 80613604 intron variant A/G snv 0.33 8
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 6
rs2072183
NPC1L1
0.925 0.040 7 44539581 synonymous variant G/A;C snv 4.0E-06; 0.25 6
rs217428
NPC1L1
7 44515974 intron variant T/G snv 0.21 0.26 1
rs217434
NPC1L1
7 44513639 synonymous variant A/G snv 0.16 0.17 1