Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs9393903
ELOVL2 ; ELOVL2-AS1
6 11042676 intron variant G/A snv 0.18 3
rs9358356
CDKAL1
1.000 0.080 6 20667151 intron variant T/C snv 0.39 1
rs9332998
CYP4A11
1 46938514 intron variant T/C snv 0.16 2
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs8396
ETFDH ; PPID
4 158709665 3 prime UTR variant T/C snv 0.29 3
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 2
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs7760535
REV3L ; MFSD4B
6 111425880 intron variant G/C snv 0.46 3
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 3
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 3
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 4
rs7094971
SLC16A9
0.925 0.120 10 59689806 intron variant A/G snv 0.13 4
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 2
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs662138
SLC22A1
6 160143444 intron variant C/G snv 0.14 2
rs6558295
GPAA1
8 144084619 intron variant C/G snv 8.1E-02 0.14 2
rs6499165
SLC7A6OS ; SLC7A6
16 68292297 non coding transcript exon variant A/C snv 0.80 2
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 4
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7