Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 7
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 5
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 5
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 3
rs2877716
ADCY5
3 123375604 intron variant T/C snv 0.76 3
rs7102710
SPON1
11 14244067 intron variant T/C snv 0.10 3
rs12243326
TCF7L2
0.925 0.160 10 113029056 intron variant T/C snv 0.27 3
rs7936247 1.000 0.040 11 92956866 intergenic variant G/T snv 0.37 2
rs853789
ABCB11
2 168944978 intron variant A/G;T snv 0.75 2
rs17683011
SLC5A1
1.000 0.120 22 32049959 missense variant A/G snv 4.8E-02 4.5E-02 2
rs17271340
VPS13C
15 62055686 intron variant C/T snv 0.33 2
rs2042608
VPS13C
15 61940181 intron variant C/A snv 0.48 2
rs13421358 2 43020088 regulatory region variant C/T snv 0.40 1
rs927332 6 6331640 intergenic variant T/C snv 0.48 1
rs3741151
ARHGEF17 ; LOC100287837
11 73309801 missense variant G/A;C;T snv 8.1E-06; 8.0E-02 1
rs78714016
CLEC10A
17 7078084 missense variant G/A;T snv 4.0E-03 1
rs17681684
GLP2R
17 9889451 missense variant G/A;C snv 0.22; 4.0E-06 1
rs150112597
HOXD1 ; HAGLR
2 176189453 missense variant G/C;T snv 2.4E-03; 4.1E-06 1
rs4746822
LOC101928994 ; HKDC1
10 69223185 non coding transcript exon variant C/T snv 0.59 1
rs201111080
PAPPA2
1 176670971 missense variant G/T snv 1.9E-04 1.8E-04 1