Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5063
CLCN6 ; NPPA-AS1 ; NPPA
0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 12
rs5065
NPPA ; CLCN6 ; NPPA-AS1
0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs12041331
PEAR1
0.776 0.200 1 156899922 intron variant G/A snv 0.19 11
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 11
rs4846049
C1orf167 ; MTHFR
0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 11
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 8
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 8
rs5082
APOA2
0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 7
rs7553007 0.827 0.120 1 159728759 intergenic variant G/A snv 0.31 7
rs1044925
SOAT1
0.827 0.120 1 179354603 3 prime UTR variant C/A;G snv 6
rs12567209 0.807 0.080 1 162066689 upstream gene variant G/A snv 8.6E-02 6
rs2306235
PLEKHO1
0.827 0.040 1 150150942 missense variant C/G;T snv 1.1E-02; 1.6E-05 4.4E-03 6
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs7211
TXNIP
0.827 0.200 1 145993449 3 prime UTR variant G/A;C;T snv 6
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs142648132
MTR
0.827 0.160 1 236816521 missense variant G/A;C;T snv 8.4E-04; 2.4E-05 5
rs5938
PTAFR
0.827 0.200 1 28150351 missense variant G/T snv 8.0E-03 2.5E-03 5
rs7212
TXNIP
0.851 0.120 1 145992816 3 prime UTR variant G/C snv 0.16 5
rs9332978
CYP4A11
0.882 0.040 1 46942278 upstream gene variant T/C snv 7.3E-02 5
rs313152
PTAFR
0.851 0.120 1 28149490 3 prime UTR variant T/C snv 0.29 4
rs3931020 0.882 0.040 1 74769633 downstream gene variant T/C snv 0.71 4