Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1801278
IRS1
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs6471
CYP21A2
0.683 0.360 6 32040110 missense variant G/A;C;T snv 1.2E-05; 5.3E-03 24
rs6688832
H6PD
0.752 0.440 1 9263851 missense variant G/A;C snv 0.28; 1.2E-04 10
rs2281939
SORBS1
0.790 0.320 10 95414595 missense variant T/C snv 8.2E-02 0.13 9
rs13405728
STON1-GTF2A1L ; LHCGR
0.790 0.200 2 48751020 intron variant A/G snv 0.15 8
rs2059807
INSR
0.851 0.200 19 7166098 intron variant A/G;T snv 7
rs4385527
AOPEP
0.827 0.280 9 94886305 intron variant G/A snv 0.31 6
rs10818854
DENND1A
0.851 0.200 9 123684499 intron variant G/A snv 5.7E-02 6
rs8111699
STK11
0.851 0.200 19 1209715 intron variant C/G snv 0.53 6
rs13429458
THADA
0.827 0.200 2 43411699 intron variant A/C snv 0.14 6
rs12478601
THADA
0.851 0.200 2 43494369 intron variant C/T snv 0.61 5
rs34603401
H6PD
0.882 0.280 1 9245386 missense variant A/C snv 0.12 0.10 4
rs2282440
SDC3
0.882 0.240 1 30874473 missense variant G/A;C snv 9.3E-02 4
rs2414096
CYP19A1 ; MIR4713HG
0.882 0.240 15 51237582 intron variant G/A snv 0.40 3
rs2491132
SDC3
0.925 0.240 1 30876800 missense variant C/A;G;T snv 8.3E-06; 0.15 3
rs10986105
DENND1A
0.925 0.200 9 123787676 intron variant T/G snv 6.9E-02 2
rs2930961
FSBP ; RAD54B
0.925 0.200 8 94431578 3 prime UTR variant T/C snv 0.35 2
rs1489441940
PTPN1
0.925 0.200 20 50510548 missense variant C/G;T snv 6.4E-06; 4.5E-05 2
rs140510483
CD44
1.000 0.160 11 35206198 missense variant A/G snv 4.4E-03 1.4E-03 1