OLFM4, olfactomedin 4, 10562

N. diseases: 89; 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: rs12552
rs12552 		1.000 0.040 13 53051646 3 prime UTR variant A/G snv 0.58
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 4 2016 2019
dbSNP: rs12552
rs12552 		1.000 0.040 13 53051646 3 prime UTR variant A/G snv 0.58
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs12552
rs12552 		1.000 0.040 13 53051646 3 prime UTR variant A/G snv 0.58
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs8181889
rs8181889 		1.000 0.040 13 53039855 intron variant G/A snv 0.46
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs9568797
rs9568797 		0.851 0.080 13 53039424 intron variant C/G;T snv
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1 		Nutritional and Metabolic Diseases; Nervous System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs9568797
rs9568797 		0.851 0.080 13 53039424 intron variant C/G;T snv
CUI: C1842675
Disease: AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder) 		0.700 1.000 1 2014 2014
dbSNP: rs9568797
rs9568797 		0.851 0.080 13 53039424 intron variant C/G;T snv
CUI: C3542025
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE 		0.700 1.000 1 2014 2014
dbSNP: rs9568797
rs9568797 		0.851 0.080 13 53039424 intron variant C/G;T snv
CUI: C1862941
Disease: Amyotrophic Lateral Sclerosis, Sporadic
Amyotrophic Lateral Sclerosis, Sporadic 		Nutritional and Metabolic Diseases; Nervous System Diseases 0.700 1.000 1 2014 2014