Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121908120
WNT10A
0.701 0.280 2 218890289 missense variant T/A snv 1.4E-02 1.4E-02 11
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs34560261
SEMA4B
0.882 0.040 15 90191194 intron variant C/T snv 0.12 3
rs10911268 1.000 0.040 1 183153583 intergenic variant C/A snv 0.39 1
rs1092479 1.000 0.040 2 121011861 intergenic variant G/C snv 0.39 1
rs1159268 1.000 0.040 1 218671564 regulatory region variant G/A snv 0.32 1
rs2727365 1.000 0.040 11 13089937 intron variant G/A;T snv 1
rs2901000 1.000 0.040 2 60274081 intergenic variant A/G snv 0.62 1
rs330071 1.000 0.040 8 9302385 intron variant G/A snv 0.25 1
rs38055 1.000 0.040 5 53264814 intergenic variant A/G snv 0.75 1
rs4487353 1.000 0.040 4 123332634 intergenic variant G/A snv 0.53 1
rs478304 1.000 0.040 11 65726789 upstream gene variant G/T snv 0.54 1
rs629725 1.000 0.040 5 53335237 TF binding site variant T/C snv 0.74 1
rs6684868 1.000 0.040 1 218674648 TF binding site variant G/A snv 0.41 1
rs75430906 1.000 0.040 3 20676437 intron variant G/A snv 1.9E-02 1
rs788790 1.000 0.040 1 202320478 downstream gene variant C/A snv 0.44 1
rs17651189
ADORA2A-AS1
1.000 0.040 22 24448915 intron variant T/C snv 2.9E-02 1
rs28360612
ADORA2A-AS1
1.000 0.040 22 24487250 intron variant T/A snv 0.20 1
rs747650
C11orf49
1.000 0.040 11 47154454 non coding transcript exon variant C/T snv 0.34 1
rs7531806
C1orf112 ; LOC107985745
1.000 0.040 1 169681903 intron variant G/A snv 0.61 1
rs2242095
EEF1D ; TIGD5
1.000 0.040 8 143596704 5 prime UTR variant C/T snv 0.15 1
rs28570522
LOC102723313 ; PINX1
1.000 0.040 8 10773058 intron variant A/G snv 0.66 1
rs158639
LOC105378977
1.000 0.040 5 56315883 intron variant G/A snv 0.33 1
rs11118336
LYPLAL1-AS1
1.000 0.040 1 219547941 intergenic variant C/T snv 0.51 1
rs1256580
LYPLAL1-DT
1.000 0.040 1 219026038 intron variant G/C snv 0.29 1