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: rs1077989
rs1077989
GPHN ; TMEM229B
1.000 0.080 14 67509105 intron variant A/C snv 0.39
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.800 1.000 1 2012 2012
dbSNP: rs17104363
rs17104363
GPHN ; TMEM229B
14 67472766 3 prime UTR variant T/C snv 0.11
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012