Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs149454410
SLC2A9
0.925 0.120 4 9942000 missense variant C/G;T snv 4.0E-05; 3.2E-04 5
rs143193096
IGF1R
15 98916098 missense variant G/A;C snv 8.4E-05; 4.0E-06 3
rs75248620
LOC101928008 ; SBF2
11 9887580 intron variant G/A snv 5.5E-02 1
rs4966025
IGF1R
15 98766313 intron variant G/A snv 0.60 1
rs2137683
IGF1R
0.925 0.120 15 98746409 intron variant C/G snv 0.53 1
rs59646751
IGF1R
15 98733292 intron variant G/T snv 0.31 1
rs11858316
IGF1R
0.925 0.120 15 98705800 intron variant C/T snv 0.50 1
rs12361687
LOC101928008 ; SBF2
11 9868505 intron variant G/A snv 0.27 1
rs12428035 13 95648618 upstream gene variant C/A;T snv 3
rs4918943
SORBS1
10 95519165 intron variant G/A snv 0.23 1
rs7326821 13 95415950 intergenic variant A/G snv 0.15 1
rs35353426 8 9439736 upstream gene variant C/G;T snv 1
rs7543734
BCAR3
1 93585354 intron variant G/A;C snv 1
rs7012814 8 9315848 intron variant G/A;T snv 2
rs7012637 8 9315699 intron variant G/A;C snv 3
rs913423 10 93085279 intergenic variant G/A snv 0.53 2
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 5
rs856534
EXOC6
10 93050908 intron variant G/A snv 0.51 1
rs17184313
RIN3
14 92635906 intron variant C/A;G;T snv 2
rs35629566
RIN3
14 92605972 intron variant C/G snv 0.12 2
rs7006504 8 9216713 intron variant T/C snv 0.32 1
rs13269272 8 92166732 intergenic variant T/A snv 0.10 1
rs117243822
CASP8AP2
6 89852962 intron variant T/C snv 1.1E-02 1
rs7187910 16 89671938 non coding transcript exon variant A/C;G snv 1