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: rs4977756
rs4977756
0.683 0.440 9 22068653 intron variant G/A snv 0.64
CUI: C0017638
Disease: Glioma
Glioma
0.900 0.875 2 2009 2020
dbSNP: rs4977756
rs4977756
0.683 0.440 9 22068653 intron variant G/A snv 0.64
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.810 1.000 1 2011 2014
dbSNP: rs4977756
rs4977756
0.683 0.440 9 22068653 intron variant G/A snv 0.64
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.800 1.000 1 2011 2011
dbSNP: rs4977756
rs4977756
0.683 0.440 9 22068653 intron variant G/A snv 0.64
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms
0.700 1.000 2 2009 2012
dbSNP: rs4977756
rs4977756
0.683 0.440 9 22068653 intron variant G/A snv 0.64
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
Nasopharyngeal Neoplasms
0.700 1.000 1 2016 2016