SYT9, synaptotagmin 9, 143425

N. diseases: 11; N. variants: 3
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10769780
rs10769780 		11 7345864 intron variant T/C snv 0.25
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.800 1.000 1 2012 2012
dbSNP: rs4369384
rs4369384 		11 7422666 intron variant A/G snv 0.64
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.700 1.000 1 2008 2008
dbSNP: rs11041321
rs11041321 		11 7332638 intron variant C/T snv 1.0E-01
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2017 2017