Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs275645 3 148746667 downstream gene variant G/A snv 0.43 1
rs3025010
VEGFA
6 43779840 non coding transcript exon variant T/C;G snv 1
rs34571439
RBP4 ; FFAR4
10 93591553 intron variant A/C snv 0.24 1
rs351219
STRA6
15 74196866 intron variant T/C snv 0.44 1
rs3741845
TAS2R9
12 10809516 missense variant A/G snv 0.60 0.51 1
rs4820294
LGALS1
22 37675036 upstream gene variant G/A snv 0.30 1
rs4917356
RXRA
9 134365597 intron variant T/C;G snv 0.15 1
rs587780343
GCK
7 44145638 missense variant C/A;T snv 1
rs587780347
GCK ; LOC105375258
7 44147807 missense variant C/T snv 1
rs6938256
CDKAL1
6 20887723 intron variant G/A;T snv 1
rs7091052
RBP4 ; FFAR4
10 93595641 intron variant G/A snv 0.15 1
rs7094463
TCF7L2
10 112952224 intron variant A/G snv 0.57 1
rs712699
PAX4
7 127610543 3 prime UTR variant G/A snv 0.75 1
rs7598922
DHX57
2 38855202 missense variant T/C snv 0.62 0.54 1
rs7929804
KCNQ1OT1 ; KCNQ1
11 2619594 non coding transcript exon variant G/A snv 0.49 1
rs909221872
ACOT7
1 6349856 missense variant G/T snv 1
rs9292578
PRLR
5 35229973 intron variant C/A;G snv 1
rs9645501
LOC101928994 ; HKDC1
10 69227010 intron variant G/A snv 0.43 1
rs3789678
AGT
1.000 0.040 1 230713736 intron variant C/T snv 0.15 5
rs7936247 1.000 0.040 11 92956866 intergenic variant G/T snv 0.37 5
rs192902098
PDX1
1.000 0.040 13 27920235 missense variant C/A;G;T snv 2.6E-03; 3.4E-04; 5.6E-05 3
rs4721
LRRC61 ; RARRES2
1.000 0.040 7 150338437 missense variant T/A;C;G snv 0.42 0.47 2
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 9