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: rs10406327
rs10406327
PEPD
1.000 0.080 19 33399932 intron variant C/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10421414
rs10421414
INSR
19 7133924 intron variant T/C snv 0.19
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1042164
rs1042164
IER2
19 13153584 missense variant C/T snv 0.13 0.13
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10435093
rs10435093 		7 25246386 intergenic variant A/T snv 0.22
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1044145
rs1044145
PFKFB2 ; YOD1
1 207044014 3 prime UTR variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1044299
rs1044299
PAPPA2
1 176842737 3 prime UTR variant C/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10448080
rs10448080
EXTL3
8 28747274 intron variant T/C snv 0.34
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2015 2015
dbSNP: rs10456943
rs10456943 		6 121556819 regulatory region variant A/C snv 0.11
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10463076
rs10463076 		5 160177301 intergenic variant G/A snv 0.16
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10467109
rs10467109
ATF7 ; ATF7-NPFF
12 53577542 intron variant C/T snv 0.17
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10467747
rs10467747
TC2N
14 91858114 intron variant C/T snv 0.70
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1046943
rs1046943
ZBTB24 ; MICAL1
1.000 0.040 6 109462738 3 prime UTR variant A/G snv 0.52
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2010 2010
dbSNP: rs1047014
rs1047014
ID4
6 19841262 3 prime UTR variant T/C snv 0.23
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2010 2010
dbSNP: rs1047891
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10479944
rs10479944 		7 15074211 intergenic variant T/A snv 0.13
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10482795
rs10482795
TGFB2
1 218432267 intron variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10483623
rs10483623
LOC105370504
14 53623359 intron variant T/G snv 0.16
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1049232
rs1049232
TRIP10
19 6751282 missense variant T/G snv 0.20 0.22
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10492321
rs10492321
SOCS2
12 93586312 downstream gene variant T/A snv 0.20
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2013 2013
dbSNP: rs10496091
rs10496091
USP34
2 61255126 intron variant G/A snv 0.29
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1049927
rs1049927
TXN
9 110256475 5 prime UTR variant T/C snv 9.5E-02 9.2E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10500834
rs10500834
SPTY2D1
11 18617165 intron variant A/T snv 0.55
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10505258
rs10505258
TRPS1
8 115590628 intron variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10505629
rs10505629
ZFAT
8 134696371 intron variant T/C snv 8.1E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1050969
rs1050969
KLF10
8 102649502 3 prime UTR variant T/C snv 9.7E-03
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019