Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs56149945
NR3C1
0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs7799039
LOC105375494
0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs80356616
KCNJ11
0.732 0.360 11 17387917 missense variant C/T snv 19
rs80356624
KCNJ11
0.752 0.240 11 17387490 missense variant C/A;T snv 16
rs4644
LGALS3
0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 11
rs1320702652
MFAP1
0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs80356618
KCNJ11
0.807 0.200 11 17387595 missense variant C/A;T snv 8
rs518147
HTR2C
0.807 0.200 X 114584109 5 prime UTR variant C/A;G snv 7
rs137853238
HNF1A
0.807 0.200 12 120994265 missense variant G/A snv 6
rs146488435
KCNH6
0.851 0.080 17 63533914 missense variant C/G;T snv 8.0E-06; 6.4E-05 5
rs561017686
NEUROD1 ; CERKL
0.882 0.120 2 181678138 missense variant G/A;C snv 8.0E-06; 8.4E-04 4
rs764232985
GCK
0.851 0.080 7 44153381 missense variant C/G;T snv 4.0E-06 4
rs1057524902
GCK
0.882 0.080 7 44145495 splice donor variant A/T snv 3
rs1057524904
LOC105375258 ; GCK
0.882 0.080 7 44147765 missense variant G/A snv 3