Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10833
IL15
0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs10835211
BDNF ; BDNF-AS
1.000 0.080 11 27679818 intron variant G/A snv 0.19 3
rs10838725
CELF1
0.925 0.160 11 47536319 intron variant T/C snv 0.22 2
rs10838738
MTCH2
1.000 0.080 11 47641497 intron variant A/G snv 0.28 6
rs10852521
FTO
1.000 0.080 16 53771053 intron variant T/A;C snv 2
rs10859525
SOCS2-AS1
1.000 0.080 12 93554681 intron variant G/A snv 0.43 1
rs10865170
LOC105374506
1.000 0.080 2 41534660 intergenic variant C/A snv 0.32 1
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 6
rs10875976
BCDIN3D-AS1
1.000 0.080 12 49832684 intron variant G/A snv 0.41 1
rs10885406
TCF7L2
0.925 0.120 10 113017965 intron variant A/G snv 0.55 2
rs10891319
SDHD
1.000 0.080 11 112096881 intron variant A/G snv 0.31 1
rs10891644
NNMT
1.000 0.080 11 114284735 intron variant G/T snv 0.52 1
rs10895068
PGR ; PGR-AS1
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs10919774 1.000 0.080 1 199938588 intergenic variant A/G snv 5.2E-02 1
rs10934857
GATA2
1.000 0.080 3 128480819 3 prime UTR variant G/A snv 0.23 1
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs10953454
LHFPL3
1.000 0.080 7 104863366 intron variant G/A snv 0.12 1
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 10
rs11039155
NR1H3
0.827 0.400 11 47259211 5 prime UTR variant G/A snv 0.14 0.12 6
rs11042023
TRIM66
1.000 0.080 11 8640969 missense variant T/C snv 0.60 0.59 3
rs11075985
FTO
1.000 0.080 16 53771295 intron variant C/A snv 0.42 3