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: rs16828074
rs16828074
NCL
1.000 0.040 2 231454043 3 prime UTR variant C/G;T snv
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.800 1.000 1 2013 2013
dbSNP: rs10202701
rs10202701
NCL
2 231463970 5 prime UTR variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs6737291
rs6737291
NCL
2 231464848 intron variant T/C snv 0.52
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7598759
rs7598759
NCL ; SNORD20 ; SNORA75
1.000 0.120 2 231457245 non coding transcript exon variant C/T snv 0.45 0.46
CUI: C0018781
Disease: Noise-induced hearing loss
Noise-induced hearing loss 		0.700 1.000 1 2015 2015