Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111942351 1.000 0.080 5 143693985 intron variant A/G snv 2.3E-02 1
rs11610782 1.000 0.080 12 125711743 intergenic variant G/A snv 2.3E-02 1
rs116133558 1.000 0.080 1 203747715 downstream gene variant C/T snv 2.7E-02 1
rs116791765 1.000 0.080 11 94347083 intergenic variant T/G snv 2.3E-02 1
rs140743827 1.000 0.080 1 165016519 intergenic variant G/A snv 2.9E-02 1
rs2687855 1.000 0.080 3 145768292 regulatory region variant G/A snv 0.71 1
rs72699765 1.000 0.080 15 25584050 downstream gene variant G/A snv 7.7E-02 1
rs75108997 1.000 0.080 1 233818485 intergenic variant G/A snv 1.8E-02 1
rs999944 1.000 0.080 2 64822719 intergenic variant A/G snv 0.83 1
rs4686803
ADIPOQ ; ADIPOQ-AS1
1.000 0.080 3 186856550 3 prime UTR variant C/T snv 0.10 1
rs35329661
ARRB1
1.000 0.080 11 75263946 3 prime UTR variant C/T snv 1.5E-02 1
rs35424364
CCDC162P
1.000 0.080 6 109322402 intron variant -/T delins 1
rs3756416
CCL28
1.000 0.080 5 43383400 intron variant T/C;G snv 1
rs7727047
CCL28
1.000 0.080 5 43374831 downstream gene variant T/A;C snv 1
rs78897171
CDH4
1.000 0.080 20 61868195 intron variant G/A snv 4.8E-02 1
rs12518414
GHR
1.000 0.080 5 42721976 downstream gene variant G/A snv 0.22 1
rs4517
GNGT1 ; TFPI2
1.000 0.080 7 93886681 3 prime UTR variant T/A;G snv 1
rs9526240
HTR2A
1.000 0.080 13 46857336 intron variant G/A snv 0.19 1
rs3790435
LEPROT ; LEPR
1.000 0.080 1 65420715 5 prime UTR variant T/A;C;G snv 0.51 1
rs11588454
LINC02770
1.000 0.080 1 191832003 intron variant T/C snv 0.33 1
rs11897825
LOC100507562
1.000 0.080 2 21471579 intron variant A/G snv 0.54 1
rs148024591
LOC105370982
1.000 0.080 15 93371222 intron variant C/T snv 2.8E-02 1
rs10433310
MIF-AS1
1.000 0.080 22 23896636 intron variant G/A snv 0.32 1
rs2033354
NBAS
1.000 0.080 2 15076492 intergenic variant T/C snv 0.30 1
rs10097555
NRG1
1.000 0.080 8 32488779 intron variant G/A snv 0.62 1