Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 9
rs12086634
HSD11B1-AS1 ; HSD11B1
0.827 0.280 1 209706914 intron variant T/G snv 0.21 0.20 6
rs52820871
MC4R
0.827 0.160 18 60371599 missense variant T/G snv 6.9E-03 7.6E-03 6
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs1063355
HLA-DQB1-AS1 ; HLA-DQB1
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 5
rs1408888
DACH1
0.851 0.120 13 71854515 intron variant T/G snv 0.30 5
rs3211938
CD36
0.882 0.200 7 80671133 stop gained T/G snv 6.2E-03 2.6E-02 5
rs6564851 0.882 0.120 16 81230992 intergenic variant T/G snv 0.48 5
rs805304
CLIC1 ; DDAH2
0.851 0.240 6 31730311 5 prime UTR variant T/G snv 0.48 5
rs9289231
KALRN
0.827 0.120 3 124055231 intergenic variant T/G snv 0.15 5
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 4
rs9402571 0.882 0.080 6 134167822 downstream gene variant T/G snv 0.22 4
rs4458523
WFS1
1.000 0.080 4 6288259 intron variant T/G snv 0.61 3
rs587780346
LOC105375258 ; GCK
0.925 0.080 7 44149823 missense variant T/G snv 3
rs6662618 0.882 0.200 1 92469854 downstream gene variant T/G snv 0.75 3
rs2908279 1.000 0.080 7 44135258 downstream gene variant T/G snv 0.59 2
rs8108269 1.000 0.080 19 45655255 downstream gene variant T/G snv 0.35 2
rs10011540
UCP1
1.000 0.080 4 140568842 5 prime UTR variant T/G snv 0.10 1
rs10882095
KIF11
1.000 0.080 10 92634645 intron variant T/G snv 0.30 1
rs11196192
TCF7L2
1.000 0.080 10 113022528 intron variant T/G snv 6.1E-02 1
rs11254375
CUBN
1.000 0.080 10 17117193 intron variant T/G snv 0.30 1
rs11619726 1.000 0.080 13 36601856 intergenic variant T/G snv 1.2E-02 1
rs11753081
CDKAL1
1.000 0.080 6 20705359 intron variant T/G snv 0.19 1
rs12111351
CDKAL1
1.000 0.080 6 20724327 intron variant T/G snv 0.34 1
rs13098494
UBE2E2
1.000 0.080 3 23374206 intron variant T/G snv 0.10 1