Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 8
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 8
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 7
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 7
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 7
rs9356744
CDKAL1
0.882 0.120 6 20685255 intron variant T/C snv 0.42 7