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: rs10748128
rs10748128 		12 69433878 intergenic variant G/T snv 0.42
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 5 2010 2019
dbSNP: rs11205277
rs11205277 		1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 5 2008 2019
dbSNP: rs1776897
rs1776897 		6 34227234 regulatory region variant G/T snv 0.80
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 5 2008 2019
dbSNP: rs1490384
rs1490384 		6 126530014 intron variant C/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2010 2019
dbSNP: rs2079795
rs2079795 		17 61419288 regulatory region variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2010 2019
dbSNP: rs6918981
rs6918981 		6 34270737 intron variant G/A snv 0.69
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2009 2019
dbSNP: rs7319045
rs7319045 		13 91372320 intergenic variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2010 2019
dbSNP: rs9428104
rs9428104 		1 118312964 intergenic variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2010 2019
dbSNP: rs1884897
rs1884897 		20 6632185 regulatory region variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2014 2019
dbSNP: rs1926872
rs1926872 		1 184049341 upstream gene variant T/C snv 0.29
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2015 2019
dbSNP: rs1950500
rs1950500 		14 24361644 upstream gene variant T/C snv 0.68
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2010 2014
dbSNP: rs2145272
rs2145272 		20 6645571 intergenic variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2010 2019
dbSNP: rs2780226
rs2780226 		6 34231315 regulatory region variant C/T snv 0.80
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2010 2019
dbSNP: rs7214743
rs7214743 		17 61420691 intergenic variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2018 2019
dbSNP: rs7513464
rs7513464 		1 118307139 regulatory region variant G/C snv 0.30
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2015 2019
dbSNP: rs757608
rs757608 		17 61419916 regulatory region variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2008 2019
dbSNP: rs7697556
rs7697556 		4 72649596 intergenic variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2010 2019
dbSNP: rs7742369
rs7742369 		6 34197944 TF binding site variant A/G snv 0.30
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2010 2019
dbSNP: rs994014
rs994014 		4 81244636 intergenic variant T/C snv 0.43
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2011 2019
dbSNP: rs1007358
rs1007358 		7 46161757 intergenic variant A/G snv 0.23
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2014 2019
dbSNP: rs10460436
rs10460436 		2 231950631 intergenic variant G/A snv 5.7E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2015 2019
dbSNP: rs10472828
rs10472828 		5 32888712 non coding transcript exon variant C/T snv 0.40
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2009 2009
dbSNP: rs10878984
rs10878984 		12 69434754 intergenic variant C/T snv 0.42
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2017 2019
dbSNP: rs1173727
rs1173727 		5 32830415 intergenic variant T/C snv 0.66
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2010 2019
dbSNP: rs12198986
rs12198986 		6 7719826 regulatory region variant G/A snv 0.37
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2008 2019