Disease: Body mass index procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 5
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 5
rs11161721
COL24A1
1 86022231 intron variant C/A snv 0.27 0.27 4
rs4691380
PDGFC
4 156798972 intron variant C/T snv 0.45 4
rs113722913
LOC105371682
1 199950846 intergenic variant T/C snv 2.6E-02 3
rs12955983 1.000 0.080 18 60205756 intergenic variant A/G snv 0.20 3
rs13273088
SULF1
8 69581739 intron variant G/A snv 0.81 3
rs2300835
AKAP6
14 32738316 intron variant C/A snv 0.16 3
rs2785980
LYPLAL1-AS1
1 219527177 intergenic variant T/C snv 0.28 3
rs308971
SYN2
3 12075120 intron variant G/A snv 0.82 3
rs35747
LOC105369944
12 102518780 intergenic variant G/A snv 0.70 3
rs4646949
TAF11 ; UHRF1BP1
6 34877672 3 prime UTR variant T/C;G snv 3
rs6689335
LYPLAL1-AS1
1 219455340 intron variant T/C snv 0.31 3
rs7374732 1.000 0.080 3 23161963 regulatory region variant C/T snv 0.73 3
rs8182584
PEPD
19 33418804 intron variant T/C;G snv 3
rs912056
LOC101928004
6 6735964 intron variant A/T snv 0.66 3
rs9552416 13 18737101 downstream gene variant C/A;T snv 3
rs9841287
LOC107986040 ; LOC105376921
3 67310 intergenic variant A/G snv 0.22 3