Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs118137427 10 111217250 intergenic variant A/G snv 3.3E-02 2
rs11891554
PPM1G
2 27390750 intron variant G/A;T snv 7.1E-02 2
rs11920090
SLC2A2
1.000 0.040 3 170999732 intron variant T/A snv 0.20 5
rs12055786
RGS17
6 153109990 intron variant C/T snv 0.46 3
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 3
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1280 3 170995501 intron variant T/C snv 0.20 2
rs13023194 0.925 0.120 2 27744393 intergenic variant G/A;C snv 4
rs13404446
TRIM54
0.925 0.120 2 27296386 intron variant G/A snv 0.42 4
rs1371614
DPYSL5
2 26930006 intron variant C/T snv 0.29 3
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs1401419
CRY2
1.000 0.040 11 45858188 intron variant T/C snv 0.39 3
rs1483121 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 4
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 4
rs16913693
ELP1
9 108918079 intron variant T/G snv 8.4E-02 2
rs16980051
SYMPK
19 45842628 non coding transcript exon variant T/A;C snv 0.47 2
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 5
rs17265513
ZHX3
0.925 0.160 20 41203988 missense variant T/C snv 0.14 0.14 6
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs17712208
PROX1-AS1
1 213977102 intron variant T/A snv 2.1E-02 2
rs17762454
RREB1
0.925 0.120 6 7212967 non coding transcript exon variant C/T snv 0.25 4