Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9461407 1.000 0.040 6 27777959 downstream gene variant G/A snv 0.31 1
rs9461219
SLC17A3
0.882 0.160 6 25836699 intron variant C/G;T snv 3
rs9441956 1.000 0.040 1 221783857 intergenic variant C/T snv 0.52 2
rs9420
SELENOH ; TMX2-CTNND1
1.000 0.040 11 57742822 non coding transcript exon variant A/G snv 0.68 1
rs9398171
FOXO3
1.000 0.040 6 108662324 intron variant C/T snv 0.55 2
rs9384900
HDAC2-AS2 ; LOC107986638
1.000 0.040 6 114389931 intron variant T/C snv 0.77 1
rs9379780 1.000 0.040 6 25706943 intergenic variant G/A snv 0.61 1
rs9375031 1.000 0.040 6 97968029 intron variant C/T snv 0.57 2
rs9372208
CCDC162P
1.000 0.040 6 109274965 intron variant A/G;T snv 2
rs9371912 1.000 0.040 6 155673423 intergenic variant G/T snv 0.19 2
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 6
rs9368481
LINC00240
1.000 0.040 6 26993982 intron variant C/T snv 0.36 2
rs9362395 1.000 0.040 6 87144623 intergenic variant T/C snv 5.4E-02 1
rs9354352 0.882 0.040 6 65986379 intergenic variant T/C snv 0.42 3
rs9348739
LINC00240 ; GUSBP2
1.000 0.040 6 26955320 intron variant G/A;C snv 2
rs9347865
LOC107986667
0.925 0.040 6 164507108 intergenic variant G/A;T snv 2
rs9331896
CLU ; MIR6843
0.851 0.080 8 27610169 intron variant C/G;T snv 1
rs9331888
CLU ; MIR6843
0.827 0.200 8 27611345 5 prime UTR variant C/G snv 0.35 0.28 1
rs9330316
RANBP2
1.000 0.040 2 109526659 intergenic variant A/G snv 0.31 1
rs9307440 1.000 0.040 4 117743348 intergenic variant G/A snv 0.55 1
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs9293741 1.000 0.040 5 78328190 regulatory region variant T/A;C snv 1
rs9292918
HCN1
1.000 0.040 5 45300933 intron variant T/C;G snv 2
rs929255 1.000 0.040 7 25233001 upstream gene variant C/T snv 0.37 1
rs9291547
PCDH7
1.000 0.040 4 30748032 intron variant A/G;T snv 1