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: rs9995997
rs9995997
4 72661796 intergenic variant G/A snv 0.36
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 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: rs998203
rs998203
6 160096856 intron variant C/T snv 0.45
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs9976812
rs9976812
21 38318323 intergenic variant C/G snv 0.39
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs9969804
rs9969804
9 92666838 intron variant A/C snv 0.68
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2010 2010
dbSNP: rs9967417
rs9967417
DYM
18 49433130 intron variant G/C;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 2 2010 2013
dbSNP: rs9956387
rs9956387
18 47247011 missense variant A/G;T snv 0.48
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs9954741
rs9954741
18 23459429 intron variant G/A;C snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2018 2018
dbSNP: rs994533
rs994533
2 217419555 intron variant G/C snv 0.39
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2014 2014
dbSNP: rs994532
rs994532
2 217419487 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs9941239
rs9941239
16 84954341 intergenic variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs9940899
rs9940899
16 69136024 intron variant T/C snv 0.32
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 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: rs9921222
rs9921222
0.925 0.120 16 325782 intron variant C/T snv 0.51
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs991967
rs991967
1 218442109 3 prime UTR variant A/C snv 0.37
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 2 2014 2019
dbSNP: rs9912468
rs9912468
17 66322239 intron variant G/A;C snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2018 2018
dbSNP: rs9909247
rs9909247
17 77378449 intron variant T/C snv 0.22
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs9904970
rs9904970
17 63123997 intron variant G/A snv 0.32
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs9903269
rs9903269
17 39586130 intergenic variant A/T snv 0.76
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs9902820
rs9902820
17 58560184 intron variant A/C;G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs9901941
rs9901941
17 45179096 intergenic variant T/A snv 0.29
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2017 2017
dbSNP: rs9901434
rs9901434
17 75392689 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs9900387
rs9900387
17 78168323 upstream gene variant A/C;G snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs989657
rs989657
12 24013492 intron variant T/C snv 0.55
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs989393
rs989393
9 98981054 intron variant T/C snv 0.35
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019