Source: GWASDB ×
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 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 9
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 7
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs1919128
C2orf16
0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 6
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 6
rs3749147
GPN1 ; CCDC121
0.882 0.120 2 27629051 missense variant G/A snv 0.23 0.20 6
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 5
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 5
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 5
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 5
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 4
rs13023194 0.925 0.120 2 27744393 intergenic variant G/A;C snv 4
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 4
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 4
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4