Disease: Multiple Sclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9275523 0.925 0.160 6 32707217 upstream gene variant C/A snv 0.27 2
rs9275765 0.925 0.160 6 32721547 downstream gene variant A/T snv 0.74 2
rs9275772 0.925 0.160 6 32721726 downstream gene variant T/C snv 0.74 2
rs9275793 0.925 0.160 6 32722250 downstream gene variant G/A snv 0.74 2
rs13017599
NONOP2
0.882 0.160 2 60937196 non coding transcript exon variant G/A snv 0.25 3
rs2040406
HLA-DQA1
0.882 0.240 6 32635230 intron variant A/G snv 0.23 3
rs2076533
BTNL2 ; TSBP1-AS1
0.882 0.200 6 32395750 intron variant C/T snv 0.40 3
rs2242665
CYP21A2 ; SLC44A4
0.882 0.160 6 31871532 missense variant C/T snv 0.60 0.60 3
rs2395173 0.882 0.240 6 32437082 upstream gene variant A/G snv 0.62 3
rs2524089
LOC112267902 ; HLA-B ; LINC02571
0.925 0.160 6 31298745 intron variant G/T snv 0.65 3
rs2647046 0.882 0.200 6 32700559 TF binding site variant A/C snv 0.64 3
rs3115576 0.882 0.200 6 32249073 intergenic variant T/A snv 0.41 3
rs3129932
TSBP1 ; TSBP1-AS1
0.925 0.160 6 32368350 intron variant G/C snv 0.76 3
rs3129941
TSBP1 ; TSBP1-AS1
0.882 0.240 6 32369909 missense variant A/G;T snv 0.81 3
rs3130050
APOM ; BAG6
0.882 0.240 6 31650984 intron variant G/A snv 0.89 3
rs3130311 0.882 0.200 6 32249590 intergenic variant A/G;T snv 3
rs3132946
NOTCH4
0.882 0.240 6 32222251 intron variant A/G snv 0.91 3
rs3134926 0.882 0.200 6 32232370 intergenic variant C/A;G snv 3
rs3134943
AGPAT1 ; MIR6833 ; RNF5
0.882 0.240 6 32179984 intron variant T/A;C snv 0.89 3
rs3135338 0.882 0.240 6 32433440 regulatory region variant C/T snv 0.62 3
rs3763307
TSBP1-AS1 ; BTNL2
0.882 0.200 6 32406845 non coding transcript exon variant A/T snv 0.24 3
rs437179
SKIV2L ; CYP21A2
0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs5000563 0.882 0.240 6 32436358 upstream gene variant A/G snv 0.24 3
rs535586
EHMT2 ; CYP21A2
0.882 0.160 6 31892560 splice region variant T/A;C snv 0.77 3
rs644827
SLC44A4 ; CYP21A2
0.882 0.160 6 31870664 missense variant T/C snv 0.60 0.60 3