Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11920090
SLC2A2
1.000 0.040 3 170999732 intron variant T/A snv 0.20 5
rs3138708
SLC2A2
3 171009914 intron variant T/G snv 3.1E-02 2
rs5394
SLC2A2
3 171027104 intron variant G/A snv 0.15 2
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs7651090
IGF2BP2
0.925 0.080 3 185795604 intron variant A/G snv 0.39 5
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs17712208
PROX1-AS1
1 213977102 intron variant T/A snv 2.1E-02 2
rs340878
PROX1-AS1 ; PROX1
1 213983706 intron variant G/C snv 0.63 2
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 7
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs6113722
LINC00261
20 22576461 intron variant G/A;T snv 2
rs1371614
DPYSL5
2 26930006 intron variant C/T snv 0.29 3
rs1124649
TMEM214
2 27037601 missense variant G/A snv 0.32 0.35 2
rs13404446
TRIM54
0.925 0.120 2 27296386 intron variant G/A snv 0.42 4
rs4665965
MPV17
0.925 0.120 2 27313513 intron variant T/A;C snv 4
rs11891554
PPM1G
2 27390750 intron variant G/A;T snv 7.1E-02 2
rs780110
IFT172
0.925 0.120 2 27462521 intron variant G/A snv 0.56 4
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
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs13023194 0.925 0.120 2 27744393 intergenic variant G/A;C snv 4
rs2305929
RBKS ; MRPL33 ; BABAM2-AS1 ; BABAM2
1.000 0.040 2 27891044 intron variant A/G snv 0.14 4
rs11619319
PLUT
13 27913462 intron variant A/G snv 0.23 2
rs576674 1.000 0.080 13 32980164 intergenic variant G/A snv 0.69 3