Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10819937 9 101460951 intergenic variant C/G;T snv 1
rs1780324 1 21495264 intergenic variant A/G snv 0.48 1
rs36053309 1 21579111 downstream gene variant C/G;T snv 0.21 1
rs6984305 8 9320758 intron variant A/T snv 0.85 1
rs7025162 1.000 0.080 9 133290774 regulatory region variant T/C snv 0.82 1
rs7173947 15 94727238 upstream gene variant C/T snv 0.61 1
rs7186908 16 72186474 regulatory region variant G/C snv 0.26 1
rs72837690 17 7185104 downstream gene variant T/C snv 0.31 1
rs73766540 5 82427213 intergenic variant T/A;C snv 1
rs75432325 17 49872966 regulatory region variant T/A;C snv 1
rs9533177 13 42615089 intergenic variant G/T snv 0.40 1
rs16856332
ABCB11
2 168984064 intron variant T/A;G snv 1
rs7267979
ABHD12
20 25317451 intron variant A/G snv 0.58 1
rs79343853
ABO
9 133270880 intron variant T/C snv 1
rs150674717
ALDH5A1
6 24512970 intron variant G/A snv 2.0E-04 1
rs2242420
ALPL
1 21578036 3 prime UTR variant C/T snv 0.11 1
rs4654971
ALPL
1 21571410 intron variant T/C snv 7.8E-02 1
rs74614333
ALPL
1 21518031 intron variant T/A snv 0.13 1
rs7966590
B4GALNT3
12 461674 intron variant G/A;C snv 1
rs144391488
BTNL2 ; TSBP1-AS1
6 32400783 intron variant C/G;T snv 1
rs139089160
CDA
1 20592062 intron variant G/A;T snv 1
rs2229450
ECE1
1 21247229 synonymous variant G/A;C snv 0.22 1
rs143370804
EIF4G3
1 21024072 intron variant G/A snv 0.34 1
rs71357834
FAM83E
19 48604360 intron variant C/T snv 9.4E-02 1
rs281377
FUT2 ; LOC105447645
0.925 0.120 19 48703346 synonymous variant C/T snv 0.49 0.42 1