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: rs152528
rs152528
FGF1 ; SPRY4-AS1
5 142638295 intron variant C/T snv 0.28
CUI: C1383860
Disease: Cardiac Hypertrophy
Cardiac Hypertrophy 		0.700 1.000 1 2011 2011
dbSNP: rs17098760
rs17098760
SPRY4-AS1
1.000 0.080 5 142500513 intron variant C/G snv 0.19
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 1.000 1 2009 2009
dbSNP: rs959662
rs959662
SPRY4-AS1
1.000 0.120 5 142328041 intron variant A/C;G snv
CUI: C0855197
Disease: Malignant Testicular Germ Cell Tumor
Malignant Testicular Germ Cell Tumor 		0.700 1.000 1 2010 2010