Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16892496
TRHR
1.000 0.080 8 109097622 intron variant A/C;G;T snv 2
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs17024258
GNAT2
1.000 0.080 1 109604699 intron variant C/T snv 4.7E-02 1
rs1805097
IRS2
0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs10735104
TRPV4
1.000 0.080 12 109790160 intron variant C/G;T snv 1
rs2796749
AMD1
0.925 0.080 6 110873500 upstream gene variant C/A;G snv 0.80 2
rs3782889
MYL2
0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 5
rs2289277
TSLP
1.000 0.080 5 111073369 5 prime UTR variant C/A;G;T snv 3
rs553668
ADRA2A
0.807 0.160 10 111079821 3 prime UTR variant A/G;T snv 8
rs695872
ATXN2-AS ; ATXN2
0.925 0.120 12 111599125 synonymous variant G/A snv 0.79 0.61 2
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs10891319
SDHD
1.000 0.080 11 112096881 intron variant A/G snv 0.31 1
rs2419621
ACSL5
0.925 0.080 10 112375255 non coding transcript exon variant C/T snv 0.23 3
rs4833407
ALPK1
1.000 0.080 4 112390634 intron variant C/A;T snv 2
rs346074
HRH1
1.000 0.080 3 11252624 intron variant T/C snv 0.54 1
rs33977706
RMI2 ; SOCS1 ; LOC105371082
0.925 0.200 16 11256298 intron variant C/A;G;T snv 2
rs243330
SOCS1 ; RMI2 ; LOC105371082
0.851 0.240 16 11257134 intron variant C/T snv 0.49 4
rs3748024
CHCHD5
0.925 0.080 2 112588836 3 prime UTR variant C/G snv 0.41 0.35 3
rs346070
HRH1
1.000 0.080 3 11262188 3 prime UTR variant T/A;C snv 1
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs7901695
TCF7L2
0.851 0.160 10 112994329 intron variant T/C snv 0.34 6
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs10885406
TCF7L2
0.925 0.120 10 113017965 intron variant A/G snv 0.55 2
rs7924080
TCF7L2
0.925 0.120 10 113027253 intron variant T/C snv 0.55 2
rs7895340
TCF7L2
0.851 0.160 10 113041766 intron variant G/A snv 0.53 4