Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 4
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 4
rs4014195 0.882 0.200 11 65739351 intergenic variant C/G snv 0.31 3
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 3
rs679899
APOB
0.925 0.080 2 21028042 missense variant G/A snv 0.49 0.39 3
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 3
rs7754840
CDKAL1
0.807 0.200 6 20661019 intron variant G/A;C;T snv 3
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 3
rs174549
FADS2 ; FADS1
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 3
rs968567
FADS2 ; FADS1
0.851 0.240 11 61828092 intron variant C/T snv 0.11 3
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 3
rs13538
NAT8 ; ALMS1P1
1.000 0.080 2 73641201 missense variant A/G snv 0.21 0.31 3
rs6420094
SLC34A1
1.000 0.080 5 177390635 intron variant A/G snv 0.29 3
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 3
rs11078903
CDK12
17 39475671 intron variant G/A;C;T snv 2
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 2
rs9944411
FBXL20
17 39327346 intron variant T/C snv 0.32 2
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 2
rs3925584
LOC101928338
1.000 0.080 11 30738788 intergenic variant T/C snv 0.35 2
rs7805747
PRKAG2
1.000 0.080 7 151710715 intron variant G/A snv 0.26 2
rs17319721
SHROOM3
0.925 0.080 4 76447694 intron variant G/A snv 0.34 2
rs6066043
SLC13A3
1.000 0.080 20 46659814 intron variant G/A;T snv 2
rs1171614
SLC16A9
0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79 2
rs1171616
SLC16A9
0.882 0.200 10 59708831 intron variant G/T snv 0.79 2