ELOVL7, ELOVL fatty acid elongase 7, 79993

N. diseases: 13; N. variants: 4
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: rs4700393
rs4700393 		5 60802440 intron variant A/G snv 0.59
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs4700393
rs4700393 		5 60802440 intron variant A/G snv 0.59
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4700394
rs4700394 		5 60821375 intron variant A/T snv 0.57
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs6449502
rs6449502 		5 60797268 intron variant T/C snv 0.82
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs7715147
rs7715147 		1.000 0.080 5 60757393 intron variant C/A;T snv
CUI: C0037019
Disease: Shy-Drager Syndrome
Shy-Drager Syndrome 		Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs7715147
rs7715147 		1.000 0.080 5 60757393 intron variant C/A;T snv
CUI: C0393571
Disease: Multiple System Atrophy
Multiple System Atrophy 		Nervous System Diseases 0.700 1.000 1 2016 2016