Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10913469
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs12517906
rs12517906 		5 180743819 upstream gene variant C/A;T snv 0.11
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2010 2010
dbSNP: rs12970134
rs12970134 		0.790 0.280 18 60217517 intergenic variant G/A snv 0.21
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs16877106
rs16877106
ANAPC4
4 25401644 intron variant C/T snv 4.9E-02
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2011 2011
dbSNP: rs1840440
rs1840440 		18 25677222 intergenic variant T/C;G snv
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2010 2010
dbSNP: rs1973993
rs1973993 		1 96478438 intergenic variant T/C snv 0.49
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs2568958
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs2844479
rs2844479 		0.925 0.200 6 31605179 intergenic variant A/C snv 0.34
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs29941
rs29941 		1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs6499640
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs7138803
rs7138803 		0.827 0.240 12 49853685 intergenic variant G/A;T snv
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs7336332
rs7336332 		13 27484267 upstream gene variant A/G snv 0.19
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs7498665
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs7561317
rs7561317 		0.925 0.120 2 644953 intergenic variant A/G snv 0.81
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs7647305
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs8050136
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs925946
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs9313296
rs9313296 		5 165950694 intergenic variant G/C snv 0.13
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2011 2011
dbSNP: rs965178
rs965178 		18 25681256 intergenic variant T/C snv 0.53
CUI: C0005910
Disease: Body Weight
Body Weight 		0.700 1.000 1 2010 2010