Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs2229616
MC4R
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 2
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 2
rs1254319
C14orf39
1.000 14 60437039 missense variant G/A snv 0.35 0.36 1
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 1
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 1
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 3
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 2
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 2
rs4846567 1 219577375 regulatory region variant G/T snv 0.23 1
rs757608 17 61419916 regulatory region variant A/G;T snv 1
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 3
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 2
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
rs12110693
LOC105377979
6 121837124 intergenic variant G/A snv 0.23 1
rs17568628 5 76751114 intergenic variant T/C;G snv 1
rs2119690 8 20002028 intergenic variant G/A;C snv 1
rs2145272 20 6645571 intergenic variant G/A;T snv 1
rs2820464
LYPLAL1-AS1
1 219519878 intergenic variant G/A;C snv 1
rs9750952 1.000 0.080 2 238827723 intergenic variant C/T snv 0.19 1
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10