Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs243391
UBXN6
1.000 0.040 19 4449811 non coding transcript exon variant G/A snv 0.98 1
rs6675269
WDR26
0.925 0.040 1 224412564 intron variant C/A snv 0.98 2
rs10732995
TNN
1 175142438 intron variant C/T snv 0.98 1
rs1013579
C8B
1 56956811 missense variant C/T snv 0.98 0.98 1
rs3108962
NFRKB
11 129895558 5 prime UTR variant A/G snv 0.98 2
rs945347 0.925 0.040 14 83623724 intergenic variant A/G snv 0.98 2
rs7007550
LONRF1
0.925 0.040 8 12750120 intron variant C/T snv 0.98 2
rs2053762
LOC105373845
1.000 0.040 2 204472387 intron variant A/G snv 0.98 1
rs11023018
LINC02683
0.925 0.040 11 13922575 intron variant C/A snv 0.98 2
rs1885645 1.000 0.040 1 177768233 intron variant A/G snv 0.98 1
rs12472508 1.000 0.040 2 204456249 intergenic variant G/A snv 0.98 1
rs1282146 1 111060860 intergenic variant T/G snv 0.98 1
rs3112681
SRRM2 ; SRRM2-AS1
16 2753955 intron variant C/A;G;T snv 0.98 1
rs2802993 0.925 0.040 1 234905572 intron variant C/T snv 0.98 2
rs3848860
MYO18B
1.000 0.040 22 25790224 intron variant C/T snv 0.98 1
rs10741881
NELL1
0.925 0.040 11 21498856 intron variant C/T snv 0.98 2
rs7722878
NREP
0.925 0.040 5 111788981 intron variant A/G snv 0.98 2
rs2842861
SLC25A44
1.000 0.040 1 156202708 intron variant T/C snv 0.98 1
rs10403206 19 46464655 downstream gene variant T/C snv 0.98 1
rs2659584
DOCK5
0.925 0.040 8 25376873 intron variant C/T snv 0.98 2
rs3102718
SCAPER
1.000 0.040 15 76752585 intron variant C/T snv 0.98 1
rs198260 1.000 0.040 14 56714297 intron variant G/A snv 0.98 1
rs2442120
DTWD2
5 118970884 intron variant A/C snv 0.98 2
rs622180 1.000 0.040 19 56080944 downstream gene variant T/C snv 0.98 1
rs1987960
HCK
20 32062031 intron variant T/C snv 0.98 1