Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10212638
PPARGC1A
1.000 0.080 4 23864492 intron variant A/G snv 0.11 1
rs1022113606
SOD3
0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs10228456 1.000 0.080 7 15024301 intergenic variant C/T snv 0.54 3
rs10229583 1.000 0.080 7 127606849 downstream gene variant G/A snv 0.23 2
rs10231021 1.000 0.080 7 15020804 intergenic variant T/A;G snv 1
rs10244051 1.000 0.080 7 15024208 intergenic variant T/A;G snv 3
rs1024610 0.882 0.200 17 34253212 upstream gene variant T/A snv 0.85 3
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10247649
PDK4
0.925 0.080 7 95586935 non coding transcript exon variant A/G snv 0.43 2
rs10255208 0.925 0.160 7 36819038 non coding transcript exon variant A/G snv 0.46 2
rs10258074 1.000 0.080 7 15024591 intergenic variant A/T snv 0.54 1
rs10258162
LOC105375490
1.000 0.080 7 127518569 intergenic variant C/T snv 0.42 1
rs10260148
LOC105375508
1.000 0.080 7 130746210 intergenic variant C/T snv 0.27 2
rs10261386
CPED1
1.000 0.080 7 121071801 intron variant C/T snv 0.38 2
rs1027700
ATF6
1.000 0.080 1 161787246 intron variant A/T snv 0.21 1
rs10278
CALCOCO2
1.000 0.080 17 48862296 missense variant C/A;G snv 4.0E-05; 0.31 1
rs10305420
GLP1R
0.925 0.160 6 39048860 missense variant C/T snv 0.31 0.27 2
rs10305492
LOC105375046 ; GLP1R
1.000 0.080 6 39079018 missense variant G/A snv 1.0E-02 1.1E-02 2
rs1031647179
HNF4A
1.000 0.080 20 44424278 missense variant C/G;T snv 1
rs1033182
ESR1
0.882 0.160 6 151873899 intron variant G/A snv 0.26 3
rs1036483919
GCK
0.925 0.080 7 44151050 missense variant A/G snv 4.0E-06 4
rs1037733674
GCG ; LOC101929532
0.882 0.120 2 162147429 missense variant T/C snv 1.4E-05 5
rs10399931
CHI3L1
0.807 0.320 1 203186952 upstream gene variant T/A;C snv 6
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25