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: rs6091540
rs6091540
LINC01524 ; LOC105372666 ; LOC105372667
20 52471323 intron variant C/T snv 0.26
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 5 2015 2018
dbSNP: rs6477694
rs6477694 		9 109170062 upstream gene variant C/T snv 0.61
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 5 2015 2019
dbSNP: rs6804842
rs6804842
RARB
3 25064946 intron variant A/G snv 0.53
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 5 2015 2019
dbSNP: rs709400
rs709400
KLC1
14 103683138 non coding transcript exon variant A/G snv 0.30
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 5 2015 2019
dbSNP: rs9641123
rs9641123
CALCR
7 93568420 intron variant G/C snv 0.30
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 5 2015 2018
dbSNP: rs972540
rs972540 		2 206380059 intergenic variant A/G snv 0.23
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 5 2015 2019
dbSNP: rs1016287
rs1016287 		2 59078490 intron variant T/A;C;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2019
dbSNP: rs10269783
rs10269783 		7 49576607 intron variant G/A snv 0.36
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2017 2019
dbSNP: rs10733682
rs10733682
LMX1B
9 126698635 3 prime UTR variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2019
dbSNP: rs10929925
rs10929925 		2 6015425 intergenic variant C/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2019
dbSNP: rs11611246
rs11611246
WNK1
12 830314 intron variant G/T snv 0.19
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2019
dbSNP: rs11688816
rs11688816
EHBP1
2 62825913 intron variant G/A snv 0.44
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2018
dbSNP: rs11847697
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2010 2018
dbSNP: rs11866815
rs11866815
AXIN1
16 337867 intron variant C/T snv 0.29
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 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: rs1441264
rs1441264 		13 79006784 intergenic variant G/A snv 0.65
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2019
dbSNP: rs1582931
rs1582931 		5 123321505 intergenic variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2017 2019
dbSNP: rs16951275
rs16951275
MAP2K5
15 67784830 intron variant T/C snv 0.30
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2019
dbSNP: rs17001654
rs17001654
SCARB2
4 76208415 intron variant C/G snv 0.16
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2018
dbSNP: rs1808579
rs1808579
NPC1 ; RMC1
18 23524924 intron variant C/T snv 0.47
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2019
dbSNP: rs1884897
rs1884897 		20 6632185 regulatory region variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2019
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: rs2176598
rs2176598
HSD17B12
11 43842728 intron variant T/C snv 0.70
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2018
dbSNP: rs2270204
rs2270204
SWI5
9 128280455 intron variant T/G snv 0.41
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2018
dbSNP: rs2307022
rs2307022
PRMT7
16 68348075 intron variant A/G snv 0.70
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2019