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: rs10441737
rs10441737
ZNF483
9 111539305 intron variant C/T snv 0.59
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.800 1.000 1 2013 2013
dbSNP: rs10980926
rs10980926
ZNF483
9 111531354 intron variant A/G snv 0.56
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.800 1.000 1 2010 2010
dbSNP: rs10217747
rs10217747
ZNF483
9 111547655 3 prime UTR variant T/A;C snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2016 2016
dbSNP: rs10980926
rs10980926
ZNF483
9 111531354 intron variant A/G snv 0.56
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs112140014
rs112140014
PTGR1 ; ZNF483
9 111563569 3 prime UTR variant G/C snv 6.9E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7036399
rs7036399
ZNF483
9 111525145 upstream gene variant T/C;G snv 0.15
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7852169
rs7852169
PTGR1 ; ZNF483
9 111556114 intron variant C/G snv 0.15
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2019 2019
dbSNP: rs7852169
rs7852169
PTGR1 ; ZNF483
9 111556114 intron variant C/G snv 0.15
CUI: C1629609
Disease: Age at menopause
Age at menopause 		0.700 1.000 1 2018 2018
dbSNP: rs7858562
rs7858562
PTGR1 ; ZNF483
9 111562668 3 prime UTR variant A/G snv 0.52
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019