Disease: Gestational Diabetes
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
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
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
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 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
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
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
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 8
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
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 6
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 5
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 5
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 5
rs7936247 1.000 0.040 11 92956866 intergenic variant G/T snv 0.37 5
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 4