Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 8
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs2287019
QPCTL
1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 7
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 7
rs3817334
MTCH2
1.000 0.080 11 47629441 intron variant C/T snv 0.36 7
rs571312 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 7
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs10838738
MTCH2
1.000 0.080 11 47641497 intron variant A/G snv 0.28 6
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 6
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 6
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 6
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs9941349
FTO
1.000 0.080 16 53791576 intron variant C/T snv 0.34 6
rs11676272
ADCY3
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 5
rs2331841 1.000 0.080 18 60161404 upstream gene variant G/A snv 0.43 5
rs2904880
CD19 ; RABEP2
1.000 0.040 16 28933075 missense variant C/G snv 0.72 0.76 5
rs7359397
SH2B1
1.000 0.040 16 28874338 upstream gene variant C/T snv 0.28 5
rs9816226
DGKG
1.000 0.080 3 186116710 intron variant A/T snv 0.82 5
rs10458787 1.000 0.040 10 4613373 intergenic variant A/C;G snv 4
rs12444979
LOC105371116
1.000 0.080 16 19922278 intergenic variant C/T snv 0.11 4