Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 5
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 4
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 4
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 4
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 3
rs12374521
LOC107986462 ; HTR4
5 148457317 intron variant C/T snv 0.45 2
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 2
rs314268
LIN28B
6 104970103 intron variant G/A snv 0.64 2
rs4549631 6 126645162 intron variant T/C;G snv 2
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 2
rs7861820
LINC01505
9 106174393 intron variant T/C snv 0.62 2
rs9391253
LIN28B-AS1
6 104919741 intron variant A/T snv 0.29 2
rs10007754
TACR3
4 103706285 intron variant T/G snv 0.34 1
rs10019555
TACR3
4 103694124 intron variant G/A;C snv 1
rs10156597
LINC01505
9 106179228 intron variant A/T snv 0.36 1
rs1040070
LRRC53 ; FPGT-TNNI3K ; TNNI3K
1.000 0.080 1 74512186 intron variant G/A;C snv 1
rs10423674
CRTC1
19 18707093 intron variant C/A;T snv 1
rs10441737
ZNF483
9 111539305 intron variant C/T snv 0.59 1
rs10453225
LINC01505
9 106157939 intron variant G/T snv 0.36 1
rs10940138 5 67898641 intron variant C/T snv 0.21 1
rs10978430
LINC01505
9 106153728 intron variant C/T snv 0.33 1
rs10980926
ZNF483
9 111531354 intron variant A/G snv 0.56 1
rs11668344
TMEM150B
0.925 0.120 19 55322296 intron variant A/G snv 0.35 1