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: rs710841
rs710841 		4 81228677 intergenic variant C/T snv 0.37
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2009 2019
dbSNP: rs7153027
rs7153027 		14 91960878 intergenic variant A/C snv 0.44
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2008 2015
dbSNP: rs720390
rs720390 		3 185830895 intergenic variant G/A snv 0.38
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2010 2014
dbSNP: rs7282733
rs7282733 		21 34336281 intron variant C/T snv 0.49
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2017 2019
dbSNP: rs749052
rs749052 		2 231931900 intergenic variant T/C snv 7.4E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2008 2014
dbSNP: rs7534091
rs7534091 		1 118321993 intergenic variant A/G snv 0.23
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2013 2019
dbSNP: rs7763064
rs7763064 		6 142476152 intergenic variant G/A snv 0.38
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2010 2019
dbSNP: rs7870753
rs7870753 		9 96439303 intergenic variant A/G snv 0.31
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2014 2019
dbSNP: rs788867
rs788867 		4 81228852 intergenic variant T/G snv 0.42
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2010 2019
dbSNP: rs7968682
rs7968682 		12 65978100 intergenic variant G/T snv 0.56
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2012 2019
dbSNP: rs822530
rs822530 		7 148934463 intergenic variant A/T snv 0.85
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2019 2019
dbSNP: rs889014
rs889014 		5 173557111 regulatory region variant C/T snv 0.42
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2010 2015
dbSNP: rs9292468
rs9292468 		5 32818967 intergenic variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2013 2014
dbSNP: rs941873
rs941873 		10 79379706 upstream gene variant G/A snv 0.48
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2011 2019
dbSNP: rs9650315
rs9650315 		8 56243039 intergenic variant G/T snv 0.21
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2008 2014
dbSNP: rs967417
rs967417 		20 6640246 intergenic variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2008 2019
dbSNP: rs9993613
rs9993613 		4 72610297 intergenic variant T/G snv 0.42
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2014 2019
dbSNP: rs1000972
rs1000972 		20 6641070 regulatory region variant T/A;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10037743
rs10037743 		5 33163672 intron variant T/C;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10059884
rs10059884 		5 32832368 regulatory region variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10061757
rs10061757 		5 56790978 intergenic variant G/C snv 0.50
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1006660
rs1006660 		15 89340289 downstream gene variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1009404
rs1009404 		6 113405402 intergenic variant T/C snv 0.71
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10100085
rs10100085 		8 40198735 regulatory region variant C/A;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10121511
rs10121511 		9 96626342 intergenic variant A/C;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019