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: rs3791679
rs3791679
0.925 0.120 2 55869757 intron variant A/G snv 0.20
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 7 2008 2019
dbSNP: rs2284746
rs2284746
1 16980180 intron variant C/A;G snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 6 2010 2019
dbSNP: rs3791675
rs3791675
1.000 0.040 2 55884174 intron variant C/T snv 0.20
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 6 2008 2019
dbSNP: rs724016
rs724016
1.000 0.040 3 141386728 5 prime UTR variant A/G snv 0.52
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 6 2008 2019
dbSNP: rs8756
rs8756
0.882 0.200 12 65965972 3 prime UTR variant C/A snv 0.56
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 6 2008 2019
dbSNP: rs1042725
rs1042725
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 5 2007 2019
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: rs143384
rs143384
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 5 2010 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: rs2093210
rs2093210
1.000 0.040 14 60490561 intron variant C/T snv 0.45
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 5 2010 2019
dbSNP: rs4369779
rs4369779
18 23155444 intron variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 5 2014 2019
dbSNP: rs606452
rs606452
1.000 0.040 11 75565133 intron variant A/C snv 0.78
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 5 2012 2019
dbSNP: rs7466269
rs7466269
9 130588697 intron variant A/G snv 0.33
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 5 2008 2017
dbSNP: rs806794
rs806794
6 26200449 3 prime UTR variant A/G snv 0.36
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 5 2010 2019
dbSNP: rs10946808
rs10946808
1.000 0.040 6 26233159 non coding transcript exon variant A/G snv 0.26
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 4 2008 2019
dbSNP: rs11107116
rs11107116
1.000 0.080 12 93584728 downstream gene variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 4 2008 2019
dbSNP: rs11205303
rs11205303
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 4 2013 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: rs1812175
rs1812175
4 144653692 intron variant A/G snv 0.79
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 4 2008 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: rs2280470
rs2280470
15 88852395 intron variant A/G snv 0.68
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 4 2010 2017
dbSNP: rs2871865
rs2871865
15 98651667 intron variant C/G snv 0.21
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 4 2010 2019
dbSNP: rs3812163
rs3812163
6 7725527 upstream gene variant A/T snv 0.38
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 4 2010 2019
dbSNP: rs4282339
rs4282339
5 168829235 intron variant G/A snv 0.18
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 4 2010 2019