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
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 14
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 11
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 9
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 7
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 7
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 7
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 5
rs10501320
MADD ; MADD-AS1
0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 5
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 5
rs17265513
ZHX3
0.925 0.160 20 41203988 missense variant T/C snv 0.14 0.14 5
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 4
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 4
rs6235
LOC101929710 ; PCSK1
0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 4
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 4
rs6234
PCSK1 ; LOC101929710
0.851 0.160 5 96393270 missense variant G/C snv 0.27 0.24 4
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 3
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 3
rs1483121 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 3
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 3