Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12128108
AGBL4
0.925 0.040 1 49827749 intron variant C/G;T snv 3
rs1555543 1 96479241 intergenic variant A/C snv 0.55 3
rs17124318
LINC01739
1 63015059 intron variant C/A;G;T snv 3
rs17381664
ZZZ3
1.000 0.080 1 77582646 intron variant T/C snv 0.29 3
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 3
rs2785980
LYPLAL1-AS1
1 219527177 intergenic variant T/C snv 0.28 3
rs2820292
NAV1 ; IPO9-AS1
1 201815159 intron variant A/C snv 0.48 3
rs3934834
LOC105378948 ; LOC112267874
1 1070426 downstream gene variant C/T snv 0.21 3
rs516636 1 177886382 intron variant C/A snv 0.17 3
rs574367 1 177904075 intron variant G/T snv 0.16 3
rs591120
CRYZL2P-SEC16B ; SEC16B
1 177933618 missense variant G/A;C snv 4.0E-06; 0.42 3
rs6667605
LOC100996583
1.000 0.040 1 2571341 downstream gene variant C/T snv 0.53 3
rs6689335
LYPLAL1-AS1
1 219455340 intron variant T/C snv 0.31 3
rs7534091 1 118321993 intergenic variant A/G snv 0.23 3
rs7550711
GPR61
1 109540264 intron variant C/T snv 2.6E-02 3
rs823114
NUCKS1
1.000 0.040 1 205750404 upstream gene variant G/A snv 0.45 3
rs984222
TBX15
1 118961220 intron variant C/A;G snv 3
rs11165643 1 96458541 intergenic variant C/T snv 0.48 2
rs11208659
LEPR
1.000 0.080 1 65513597 intron variant T/A;C snv 0.17 2
rs11264483
C1orf61
1 156436589 intron variant G/C snv 0.45 2
rs12042959
SDCCAG8
1 243369971 intron variant A/G;T snv 2
rs12135191 1 236307434 regulatory region variant C/G;T snv 2
rs12401738
FUBP1 ; GIPC2 ; DNAJB4
1 77981077 intron variant G/A snv 0.26 2
rs12406019 1 78212446 intergenic variant A/G snv 0.32 2
rs12566985
TNNI3K ; LRRC53 ; FPGT-TNNI3K
1 74536509 intron variant G/A snv 0.42 2