Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs148121703
GABRB1
0.925 0.040 4 47371654 intron variant TGT/- delins 2.6E-03 2
rs201394051 0.925 0.040 5 117697919 intergenic variant TA/-;TATA;TATATA delins 2
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 3
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 3
rs6136
SELP
0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 3
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 3
rs11915606
BTD
0.925 0.040 3 15633655 intron variant T/G snv 3.4E-02 2
rs1870634 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 2
rs1051338
LIPA
0.807 0.120 10 89247603 missense variant T/G snv 0.32 0.26 1
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 1
rs4143832 0.925 0.080 5 132527285 intron variant T/G snv 0.76 1
rs5943057
CHRDL1
1.000 0.040 X 110695977 intron variant T/G snv 0.50 1
rs7808424
CFTR ; ASZ1
1.000 0.040 7 117427768 intron variant T/G snv 0.11 1
rs864265 0.925 0.080 3 186836503 intergenic variant T/G snv 0.86 1
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 7
rs4939883
LOC105372112
1.000 0.040 18 49640844 TF binding site variant T/C;G snv 3
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 2
rs944797
CDKN2B-AS1
0.882 0.120 9 22115287 intron variant T/C;G snv 0.49 1
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 17
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16