Disease: Glucose measurement
Source: ALL
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 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 18
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 9
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 8
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 6
rs2971672
GCK
7 44166307 intron variant A/C snv 0.44 4
rs8396
ETFDH ; PPID
4 158709665 3 prime UTR variant T/C snv 0.29 4
rs2066938
UNC119B ; MIR4700
12 120722812 3 prime UTR variant A/C;G snv 3
rs211718
SLC44A5
1 75640990 downstream gene variant T/C snv 0.75 3
rs4253252
KLKB1
4 186236304 intron variant T/G snv 0.56 3
rs7760535
REV3L ; MFSD4B
6 111425880 intron variant G/C snv 0.46 3