Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 8
rs1980493
BTNL2 ; TSBP1-AS1
0.776 0.400 6 32395438 intron variant T/C snv 0.13 6
rs9268856
HLA-DRB9
0.807 0.240 6 32461942 intron variant C/A;T snv 4
rs9268877
HLA-DRB9
0.827 0.200 6 32463370 intron variant A/G;T snv 4
rs3849942
C9orf72 ; LOC107987057
0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 2
rs2814707
LOC112268043 ; C9orf72 ; LOC107987057
0.882 0.120 9 27536399 non coding transcript exon variant C/G;T snv 2
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 2
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 1
rs769446
APOE
0.882 0.120 19 44905371 upstream gene variant T/C snv 7.0E-02 1
rs1358071
LINC02210-CRHR1
1.000 0.120 17 45725823 intron variant C/A;T snv 1
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 1
rs302668
RAB38
0.925 0.120 11 88143743 intron variant T/C snv 0.28 1