Source: GWASDB

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: rs3783637
rs3783637
GCH1
14 54881400 intron variant C/T snv 0.12
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012