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
rs10272006
SP4
0.925 0.080 7 21480514 intron variant G/A snv 0.75 3
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1057156731
LMNA
0.925 0.120 1 156137730 missense variant T/A snv 3
rs1057613
MTTP
1.000 0.040 4 99583828 3 prime UTR variant G/A snv 0.60 1
rs10750097
APOA5
1.000 0.040 11 116793324 upstream gene variant G/A;C snv 6
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs10883437 1.000 0.040 10 100035604 regulatory region variant T/A;G snv 0.43 3
rs11166927
TRAPPC9
1.000 0.040 8 139784177 intron variant T/C snv 0.39 1
rs11235972
UCP3
1.000 0.040 11 74006029 intron variant G/A snv 0.21 1
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs1131580
TNFSF10
0.882 0.160 3 172505830 3 prime UTR variant A/C;G;T snv 4
rs1137100
LEPR
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11599176
SIRT1
0.925 0.080 10 67894017 intron variant A/G snv 0.11 2
rs117542855 1.000 0.040 11 1635713 regulatory region variant C/G;T snv 3.1E-02 1
rs11794552
LOC105376299 ; PLPP7
1.000 0.040 9 131344938 intron variant C/T snv 0.15 1
rs11820744
OSBPL5 ; LOC107987158
1.000 0.040 11 3147308 intron variant C/T snv 0.23 2
rs11868035
RAI1 ; SREBF1
0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 14
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs11976006
CREB5
1.000 0.040 7 28691895 intron variant G/A snv 6.1E-02 3
rs12137855
LYPLAL1
0.882 0.040 1 219275036 downstream gene variant C/T snv 0.19 3
rs12152703
KLB
0.925 0.120 4 39420199 intron variant G/T snv 0.28 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1227756
COL13A1
0.925 0.080 10 69828748 intron variant G/A;C snv 2