Disease: Body mass index
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs6234
PCSK1 ; LOC101929710
0.851 0.160 5 96393270 missense variant G/C snv 0.27 0.24 8
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 7
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs7740107
L3MBTL3
1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56 5
rs72755233
ADAMTS17
1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 5
rs2145270 20 6641038 regulatory region variant C/T snv 0.61 4
rs34720381
PRRC2C
1 171486183 intron variant C/T snv 7.3E-02 4
rs7195386
RBBP6
0.925 0.120 16 24567137 splice region variant T/A;C snv 0.56 4
rs12449442
BPTF
17 67951524 non coding transcript exon variant G/A snv 0.22 3
rs145878042
RAPGEF3
12 47749532 missense variant A/G snv 7.3E-03 7.6E-03 3
rs1582931 5 123321505 intergenic variant G/A;T snv 3