Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 1
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 39
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 4
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 1
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 4
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 1
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 1
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 1
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 13
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 9
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7