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: rs2080454
rs2080454
16 49028679 intergenic variant C/A snv 0.54
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 4 2015 2018
dbSNP: rs2207139
rs2207139
1.000 0.080 6 50877777 intergenic variant A/G snv 0.16
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 4 2015 2017
dbSNP: rs2867125
rs2867125
0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 4 2010 2019
dbSNP: rs4986044
rs4986044
17 21358248 regulatory region variant C/T snv 0.53
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 4 2015 2018
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: rs7164727
rs7164727
15 72801650 downstream gene variant C/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 4 2015 2018
dbSNP: rs7243357
rs7243357
18 59216087 upstream gene variant T/G snv 0.18
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 4 2015 2019
dbSNP: rs7613875
rs7613875
1.000 0.040 3 49934081 upstream gene variant C/A;G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 4 2015 2018
dbSNP: rs10760279
rs10760279
9 123343012 regulatory region variant G/T snv 0.35
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2015 2018
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: rs11065987
rs11065987
0.807 0.280 12 111634620 intergenic variant A/G snv 0.29
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2015 2018
dbSNP: rs11170468
rs11170468
12 39036246 intergenic variant A/C snv 0.20
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2015 2019
dbSNP: rs11692326
rs11692326
2 207398555 intron variant C/T snv 0.18
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2015 2019
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: rs12463617
rs12463617
1.000 0.080 2 629244 regulatory region variant A/C;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2013 2019
dbSNP: rs13174863
rs13174863
5 139701160 intron variant A/G snv 0.12
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2015 2019
dbSNP: rs17513613
rs17513613
19 29795915 regulatory region variant T/C snv 0.25
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2015 2019
dbSNP: rs17782313
rs17782313
0.683 0.480 18 60183864 intergenic variant T/C snv 0.24
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2008 2017
dbSNP: rs1819844
rs1819844
12 67811824 TF binding site variant A/G snv 0.84
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2018 2019
dbSNP: rs2357760
rs2357760
6 119892734 intergenic variant G/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2017 2019
dbSNP: rs2890652
rs2890652
2 142202362 intergenic variant T/C snv 0.21
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2010 2018
dbSNP: rs571312
rs571312
1.000 0.080 18 60172536 intergenic variant C/A snv 0.26
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2010 2017
dbSNP: rs713586
rs713586
0.925 0.160 2 24935139 intergenic variant T/C snv 0.58
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2010 2019
dbSNP: rs887912
rs887912
1.000 0.080 2 59075742 intron variant T/C;G snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2010 2019
dbSNP: rs943466
rs943466
6 33764010 intergenic variant G/A snv 0.27
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2015 2018