Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12086634
HSD11B1-AS1 ; HSD11B1
0.827 0.280 1 209706914 intron variant T/G snv 0.21 0.20 6
rs4641
LMNA
0.851 0.120 1 156137743 splice region variant C/T snv 0.26 0.21 6
rs846910
HSD11B1 ; HSD11B1-AS1
0.882 0.160 1 209701909 intron variant A/G snv 0.95 6
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs17368528
H6PD
0.827 0.400 1 9264154 missense variant C/A;T snv 0.12 8.9E-02 5
rs12083537
IL6R
0.882 0.200 1 154408627 intron variant A/G snv 0.22 4
rs2282440
SDC3
0.882 0.240 1 30874473 missense variant G/A;C snv 9.3E-02 4
rs148446907
AGT
0.925 0.080 1 230710026 synonymous variant G/A;C snv 1.2E-05 3
rs164147
NOS1AP
0.882 0.080 1 162368607 3 prime UTR variant A/C snv 0.76 3
rs2774279
USF1 ; ARHGAP30
0.925 0.080 1 161047766 synonymous variant C/T snv 0.27 0.27 3
rs3093068 1.000 0.040 1 159711574 downstream gene variant G/C snv 0.13 3
rs45487298
HSD11B1-AS1 ; HSD11B1
0.882 0.120 1 209706871 intron variant -/A delins 3
rs726344
FNDC5
0.882 0.120 1 32867503 intron variant G/A snv 0.16 3
rs1000283
HSD11B1 ; HSD11B1-AS1
0.925 0.080 1 209721316 intron variant G/A snv 0.18 2
rs201844852
ETV3
0.925 0.080 1 157135581 missense variant C/G snv 4.8E-05 4.2E-05 2
rs359935 1.000 0.040 1 89517625 intron variant G/A;T snv 2
rs3818569
RXRG
0.925 0.160 1 165419892 synonymous variant G/A snv 2
rs755686359
LMNA
0.925 0.080 1 156136311 missense variant C/T snv 1.6E-05 3.5E-05 2
rs10746473
PER3
1.000 0.040 1 7817996 intron variant A/G snv 0.58 1
rs10920533
ADIPOR1
1.000 0.040 1 202956690 intron variant G/A snv 0.22 1
rs376021 1.000 0.040 1 161555218 intron variant T/C snv 1.5E-04 1
rs3790433
LEPR ; LEPROT
1.000 0.040 1 65428659 intron variant C/G;T snv 1
rs4846922
GALNT2
1.000 0.040 1 230171436 intron variant T/A;C;G snv 1
rs775276843
AGT
1.000 0.040 1 230710676 missense variant C/T snv 4.0E-06 1
rs846906
HSD11B1 ; HSD11B1-AS1
1.000 0.040 1 209714373 intron variant T/A;C snv 1