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: rs1963304
rs1963304
ZKSCAN1
7 100028173 intron variant T/A;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4486555
rs4486555 		10 100039545 downstream gene variant G/T snv 0.40
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs11599750
rs11599750
CPN1
10 100045685 intron variant C/T snv 0.40
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2010 2010
dbSNP: rs397807524
rs397807524
ADAMTS17
15 100052239 intron variant -/AA ins 7.0E-06
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs149578709
rs149578709
ADAMTS17
15 100132203 intron variant A/G snv 9.0E-03 5.2E-03
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4851253
rs4851253
AFF3
2 100146324 intron variant T/G snv 0.44
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs72755233
rs72755233
ADAMTS17
1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2017 2019
dbSNP: rs6857001
rs6857001
SLC2A9 ; LOC105374476
4 10016456 intron variant G/A snv 0.32
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs76301628
rs76301628
ADAMTS17
15 100183232 intron variant G/T snv 3.4E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4965593
rs4965593
ADAMTS17
15 100218180 intron variant C/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2013 2013
dbSNP: rs4965598
rs4965598
ADAMTS17
15 100219409 intron variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2010 2010
dbSNP: rs4533267
rs4533267
ADAMTS17
15 100246066 intron variant A/G snv 0.63
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2008 2008
dbSNP: rs4369638
rs4369638
ADAMTS17
15 100254158 synonymous variant C/T snv 0.75 0.76
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4467054
rs4467054
ADAMTS17
15 100255167 intron variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4965612
rs4965612
ADAMTS17
15 100261237 intron variant A/G snv 0.72
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs28411867
rs28411867
ADAMTS17
15 100314288 intron variant C/T snv 0.19
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs17420882
rs17420882
CDC14A
1 100353172 intron variant T/G snv 0.22
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs78352137
rs78352137
WDR25
14 100454079 intron variant T/C snv 7.7E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs9300607
rs9300607
GGACT
13 100571205 intron variant A/C;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2495739
rs2495739 		10 100575750 intergenic variant C/T snv 0.20
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: rs117182230
rs117182230
DLK1
14 100729932 intron variant C/T snv 4.0E-03
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs3783350
rs3783350
DLK1
14 100732685 intron variant G/A snv 0.64
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs3133577
rs3133577 		8 100793314 intergenic variant C/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs79990258
rs79990258
ZAN
7 100794560 intron variant T/A snv 2.4E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019