Disease: Finding of body mass index
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12525532
ANKS1A
6 35037042 intron variant C/T snv 0.33 2
rs12617233
LINC01122
2 58812863 intron variant T/A;C snv 2
rs12999687
DNMT3A
2 25289569 intron variant T/G snv 0.48 2
rs13034723
C2orf88
2 190120954 intron variant G/A snv 0.37 2
rs13078807
CADM2
0.925 0.120 3 85835000 intron variant A/G snv 0.15 5
rs13273088
SULF1
8 69581739 intron variant G/A snv 0.81 3
rs1401635
BDNF ; BDNF-AS
0.925 0.040 11 27672444 intron variant C/G snv 0.73 4
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs1514175
TNNI3K ; LRRC53 ; FPGT-TNNI3K
1.000 0.080 1 74525960 intron variant A/G snv 0.48 4
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 8
rs1542829
COL6A5
3 130418627 intron variant G/A snv 8.0E-02 3
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs16986921
CTNNBL1
1.000 0.080 20 37754119 intron variant C/T snv 0.12 3
rs17124318
LINC01739
1 63015059 intron variant C/A;G;T snv 3
rs17700144 1.000 0.080 18 60144750 intron variant G/A snv 0.14 4
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs17817964
FTO
0.925 0.120 16 53794154 intron variant C/T snv 0.30 6
rs1837269
LOC101929710
5 96523440 intron variant C/T snv 0.53 2
rs201167096
FPGT-TNNI3K ; LRRC53 ; TNNI3K
1 74534327 intron variant -/T delins 2
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 6
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs206936
RPS10-NUDT3 ; NUDT3
0.882 0.160 6 34335092 intron variant A/G snv 0.34 8
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs2206734
CDKAL1
0.882 0.160 6 20694653 intron variant C/T snv 0.20 6
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16