Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 6
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs12569232
LOC107985258
0.882 0.280 1 211379722 intron variant G/C;T snv 4
rs11209951
LOC105378797
1 72371807 intron variant C/T snv 0.61 3
rs1620977
NEGR1
1.000 0.040 1 72263459 intron variant A/G;T snv 3
rs3027001
CADM3-AS1 ; CADM3
1.000 0.040 1 159199673 intron variant C/G;T snv 3
rs3747631
LOC105371692 ; LRRN2
1.000 0.040 1 204618441 missense variant G/A;C snv 4.0E-06; 0.20 3
rs1008078 1.000 0.040 1 90724174 non coding transcript exon variant C/T snv 0.33 2
rs10783018
LOC101928219 ; LINC02607
1 95782279 non coding transcript exon variant G/A snv 0.74 2
rs10922907 1 90727492 downstream gene variant A/G;T snv 2
rs11209943
LOC105378797
1 72284817 intron variant A/G snv 0.53 2
rs11209970
FOXO6
1.000 0.040 1 41377768 intron variant G/A snv 0.59 2
rs11588857
LRRN2 ; LOC105371692
1 204617919 missense variant G/A;T snv 0.20; 8.0E-06 2
rs12124523
NEGR1
1.000 0.040 1 72155780 intron variant C/T snv 7.0E-02 2
rs12139351 1.000 0.040 1 199471855 intergenic variant G/A snv 0.21 2
rs12410444
LOC101929592 ; ST3GAL3
1.000 0.040 1 43723048 intron variant A/G snv 0.25 2
rs1343775 1 41292321 intron variant A/G snv 0.17 2
rs17043393
ESRRG
1 216698070 intron variant A/G snv 0.13 2
rs17393468 1 9378481 intergenic variant T/C snv 0.14 2
rs1831539
LINC01358
1 59094665 intron variant T/C snv 0.41 2
rs2015244 1.000 0.040 1 29956096 intergenic variant A/T snv 0.54 2
rs2143103 1.000 0.040 1 22103576 downstream gene variant G/A;T snv 2
rs2163503
ZRANB2-AS2
1 71335356 intron variant A/C snv 0.17 2
rs2256126
SDCCAG8
1.000 0.040 1 243340806 intron variant A/G snv 0.27 2