Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9994441
SH3RF1
1.000 0.080 4 169173411 intron variant G/C snv 0.19 1
rs9945493 1.000 0.080 18 78743253 intergenic variant G/A snv 4.5E-02 1
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs9934540
VAT1L
1.000 0.080 16 77842866 intron variant T/C snv 8.9E-02 1
rs9899728 1.000 0.080 17 75022679 downstream gene variant G/A snv 8.4E-02 1
rs9877502 0.925 0.080 3 190951729 intergenic variant G/A snv 0.40 1
rs983392 1.000 0.080 11 60156035 downstream gene variant A/G snv 0.28 1
rs982100 1.000 0.080 2 117717968 intergenic variant A/G snv 0.93 1
rs9749589
NFIC
1.000 0.080 19 3405594 intron variant T/A;C snv 0.17 1
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 3
rs9653111
GEMIN7-AS1 ; MARK4 ; GEMIN7
1.000 0.080 19 45089217 intron variant C/T snv 9.9E-02 1
rs9640386
EPHA1-AS1
1.000 0.080 7 143435090 intron variant G/A snv 0.50 1
rs9546312 1.000 0.080 13 83172816 intergenic variant C/T snv 0.82 1
rs9469112 1.000 0.080 6 32447376 downstream gene variant C/T snv 0.17 1
rs9468
MAPT
0.882 0.080 17 46024197 3 prime UTR variant T/C snv 0.15 0.14 1
rs9395288 1.000 0.080 6 47630389 downstream gene variant C/T snv 0.24 1
rs9395255 1.000 0.080 6 47424807 regulatory region variant T/A snv 0.35 1
rs9381563 1.000 0.080 6 47464901 intergenic variant C/A;G;T snv 1
rs9381040
LOC107986595
1.000 0.080 6 41186912 downstream gene variant C/T snv 0.29 1
rs9372110
LOC105377923
1.000 0.080 6 105869321 intron variant G/A snv 8.5E-02 1
rs9369477
SPATS1
1.000 0.080 6 44340892 intron variant T/C;G snv 1
rs9349407
CD2AP
1.000 0.080 6 47485642 intron variant G/C snv 0.23 2
rs9332739
CYP21A2 ; C2-AS1 ; C2
0.763 0.360 6 31936027 missense variant G/A;C snv 4.1E-06; 3.9E-02 5
rs9331908
CLU
1.000 0.080 8 27606101 intron variant C/T snv 0.35 1
rs9331896
CLU ; MIR6843
0.851 0.080 8 27610169 intron variant C/G;T snv 1