Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10228456 1.000 0.080 7 15024301 intergenic variant C/T snv 0.54 2
rs10747083 12 132465032 downstream gene variant G/A;T snv 2
rs11039130 11 47207765 intergenic variant C/T snv 0.20 2
rs11195502 10 111279909 intergenic variant C/A;G;T snv 2
rs11607883 11 45818158 intron variant G/A snv 0.40 2
rs11782386 8 9344277 intron variant C/T snv 9.7E-02 2
rs118137427 10 111217250 intergenic variant A/G snv 3.3E-02 2
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 2
rs1280 3 170995501 intron variant T/C snv 0.20 2
rs4775471 15 62132450 intergenic variant C/T snv 0.18 2
rs576674 1.000 0.080 13 32980164 intergenic variant G/A snv 0.69 2
rs983309 8 9320222 intron variant T/G snv 0.82 2
rs11715915
AMT
3 49417897 synonymous variant C/A;T snv 0.28 2
rs7101470
C11orf49
11 47032897 intron variant A/G snv 7.4E-02 2
rs3829109
CARD9 ; DNLZ
9 136362314 intron variant G/A snv 0.25 2
rs2390732
CERS6
2 168749457 intron variant G/A snv 0.65 2
rs1401419
CRY2
1.000 0.040 11 45858188 intron variant T/C snv 0.39 2
rs2292910
CRY2
1.000 0.080 11 45882062 3 prime UTR variant A/C snv 0.66 2
rs16913693
ELP1
9 108918079 intron variant T/G snv 8.4E-02 2
rs8020333
FOXN3
14 89568505 intron variant C/G;T snv 0.52 2
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 2
rs2268575
GCK ; LOC105375258
7 44149675 intron variant T/C snv 0.18 2
rs11672660
GIPR ; MIR642B
19 45676926 intron variant C/T snv 0.18 0.17 2
rs4237150
GLIS3
9 4290085 intron variant G/A;C;T snv 2
rs7867224
GLIS3
9 4292152 intron variant A/C;G snv 0.37 2