Source: BEFREE

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: rs9811920
rs9811920
CMSS1
1.000 0.040 3 100125449 intron variant G/A snv 0.43
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.010 < 0.001 1 2016 2016