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: 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: rs10109417
rs10109417
DPYSL2
8 26530784 intron variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1011416
rs1011416
RBMS3 ; LINC00693
3 28755186 intron variant T/C snv 0.15
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10120219
rs10120219
LOC105376158
9 95602265 intron variant C/A;T 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
dbSNP: rs10121673
rs10121673 		9 108469029 regulatory region variant C/T snv 0.32
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10128898
rs10128898
ERC1
12 1385266 intron variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10129429
rs10129429 		14 91964487 downstream gene variant G/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10131337
rs10131337
PAX9
14 36675311 intron variant C/T snv 0.19
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1013209
rs1013209 		8 24258791 intergenic variant C/T snv 0.28
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2010 2010
dbSNP: rs10132476
rs10132476
CCDC197
14 94001945 intron variant G/T snv 0.39
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10146757
rs10146757 		14 95073400 intergenic variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10150698
rs10150698
ANKRD9 ; LOC105370679
14 102511539 upstream gene variant T/C snv 0.48
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10152591
rs10152591
DRAIC ; LOC107984788
15 69755818 intron variant A/C snv 9.8E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2010 2010
dbSNP: rs10155941
rs10155941 		7 134737981 upstream gene variant T/C snv 0.43
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10157941
rs10157941
PODN
1 53083314 intron variant C/G snv 0.25
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10165255
rs10165255
CYS1
2 10059474 intron variant A/G snv 0.59
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10179158
rs10179158 		2 65784898 intron variant T/C;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10185143
rs10185143 		2 24927889 intergenic variant T/C;G snv 0.57
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10185917
rs10185917 		2 171508843 intergenic variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10187066
rs10187066
ZNF142
2 218650036 intron variant A/G snv 0.45
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2010 2010
dbSNP: rs10188078
rs10188078 		2 113694652 intron variant G/A snv 0.15
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10189857
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10192454
rs10192454
GLI2
2 120865193 intron variant G/C snv 0.60
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs10198628
rs10198628 		2 12824371 intron variant A/G snv 0.59
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017