Disease: Body mass index
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 12
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 8
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 7
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 5
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs2650492
SBK1
16 28322090 3 prime UTR variant G/A snv 0.20 5
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56 5
rs12429545 13 53528071 intron variant G/A;T snv 0.12 4
rs12885454
LOC102724934
14 29267632 non coding transcript exon variant C/A snv 0.27 4