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: rs9866391
rs9866391
1.000 0.040 3 141357242 intron variant T/C snv 0.41
CUI: C0027092
Disease: Myopia
Myopia
0.700 1.000 1 2016 2016