Source: GWASCAT

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: rs543874
rs543874 		1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 14 2010 2019
dbSNP: rs17024393
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 7 2015 2019
dbSNP: rs3101336
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 7 2015 2019
dbSNP: rs11165643
rs11165643 		1 96458541 intergenic variant C/T snv 0.48
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 6 2015 2019
dbSNP: rs10920678
rs10920678
BRINP3
1 190270777 intron variant A/G snv 0.58
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 5 2015 2019
dbSNP: rs12566985
rs12566985
TNNI3K ; FPGT-TNNI3K ; LRRC53
1 74536509 intron variant G/A snv 0.42
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2017
dbSNP: rs633715
rs633715 		1.000 0.080 1 177883445 intron variant T/C snv 0.17
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2013 2019
dbSNP: rs657452
rs657452
AGBL4
1 49124175 intron variant A/G snv 0.54
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2018
dbSNP: rs7550711
rs7550711
GPR61
1 109540264 intron variant C/T snv 2.6E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2019
dbSNP: rs10923724
rs10923724 		1 119004219 upstream gene variant C/T snv 0.53
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2017 2019
dbSNP: rs11583200
rs11583200
ELAVL4
1 50094148 intron variant C/T snv 0.48
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2015 2018
dbSNP: rs12401738
rs12401738
FUBP1 ; DNAJB4 ; GIPC2
1 77981077 intron variant G/A snv 0.26
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2015 2017
dbSNP: rs12406019
rs12406019 		1 78212446 intergenic variant A/G snv 0.32
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2015 2018
dbSNP: rs17381664
rs17381664
ZZZ3
1.000 0.080 1 77582646 intron variant T/C snv 0.29
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2015 2018
dbSNP: rs2481665
rs2481665
PATJ
1 62129005 intron variant T/C snv 0.31
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2015 2018
dbSNP: rs2568958
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2009 2019
dbSNP: rs2820292
rs2820292
NAV1 ; IPO9-AS1
1 201815159 intron variant A/C snv 0.48
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2015 2017
dbSNP: rs977747
rs977747
TAL1
1 47219005 3 prime UTR variant T/C;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2015 2018
dbSNP: rs10754220
rs10754220
CRB1
1 197275160 intron variant G/A snv 0.22
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2017 2018
dbSNP: rs10913469
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2009 2019
dbSNP: rs11185092
rs11185092
NTNG1
1 107343656 intron variant A/G snv 0.26
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2017 2018
dbSNP: rs112566467
rs112566467
MACF1
1 39096955 intron variant C/T snv 0.16
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs12042959
rs12042959
SDCCAG8
1 243369971 intron variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs12140153
rs12140153
PATJ
1 62114219 missense variant G/A;T snv 4.0E-06; 5.9E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs1514175
rs1514175
TNNI3K ; FPGT-TNNI3K ; LRRC53
1.000 0.080 1 74525960 intron variant A/G snv 0.48
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2010 2013