GPC6, glypican 6, 10082

N. diseases: 86; N. variants: 15
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: rs143258881
rs143258881 		1.000 0.080 13 93293605 intron variant A/T snv 1.5E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.800 1.000 1 2014 2014
dbSNP: rs7995215
rs7995215 		1.000 0.040 13 93756253 intron variant A/G snv 0.68
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.800 1.000 1 2008 2008
dbSNP: rs9301951
rs9301951 		1.000 0.040 13 94300578 intron variant T/C;G snv
CUI: C0158266
Disease: Intervertebral Disc Degeneration
Intervertebral Disc Degeneration 		Musculoskeletal Diseases 0.800 1.000 1 2013 2013
dbSNP: rs12430764
rs12430764 		13 93244682 intron variant G/A snv 0.58
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs1328369
rs1328369 		13 93260737 intron variant C/T snv 0.57
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2018 2018
dbSNP: rs2150127
rs2150127 		13 93838807 intron variant A/G snv 7.1E-02
CUI: C0038663
Disease: Suicide attempt
Suicide attempt 		Behavior and Behavior Mechanisms 0.700 1.000 1 2012 2012
dbSNP: rs7985891
rs7985891 		1.000 13 93226778 non coding transcript exon variant A/G snv 3.7E-02
CUI: C0442874
Disease: Neuropathy
Neuropathy 		Nervous System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs7985891
rs7985891 		1.000 13 93226778 non coding transcript exon variant A/G snv 3.7E-02
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2014 2014
dbSNP: rs7985891
rs7985891 		1.000 13 93226778 non coding transcript exon variant A/G snv 3.7E-02
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2014 2014
dbSNP: rs7985891
rs7985891 		1.000 13 93226778 non coding transcript exon variant A/G snv 3.7E-02
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2014 2014
dbSNP: rs7985891
rs7985891 		1.000 13 93226778 non coding transcript exon variant A/G snv 3.7E-02
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2014 2014
dbSNP: rs7998314
rs7998314 		13 93580876 intron variant A/C snv 0.77
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs9524298
rs9524298 		13 93980567 intron variant G/A snv 0.17
CUI: C0021655
Disease: Insulin Resistance
Insulin Resistance 		Nutritional and Metabolic Diseases 0.700 1.000 1 2012 2012
dbSNP: rs9561329
rs9561329 		1.000 0.040 13 93358916 intron variant A/G snv 0.15
CUI: C0027932
Disease: Neurotic Disorders
Neurotic Disorders 		Mental Disorders 0.700 1.000 1 2010 2010
dbSNP: rs9561329
rs9561329 		1.000 0.040 13 93358916 intron variant A/G snv 0.15
CUI: C1842981
Disease: NEUROTICISM
NEUROTICISM 		Behavior and Behavior Mechanisms 0.700 1.000 1 2010 2010
dbSNP: rs9584154
rs9584154 		1.000 0.040 13 93774100 intron variant A/G snv 0.29
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs9584224
rs9584224 		13 94403472 3 prime UTR variant G/A snv 4.0E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9584224
rs9584224 		13 94403472 3 prime UTR variant G/A snv 4.0E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs121908440
rs121908440 		1.000 0.120 13 93830534 stop gained C/T snv 4.0E-06
CUI: C1850318
Disease: Omodysplasia type 1
Omodysplasia type 1 		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.700 0
dbSNP: rs863223282
rs863223282 		1.000 0.120 13 94027795 frameshift variant C/- del
CUI: C1850318
Disease: Omodysplasia type 1
Omodysplasia type 1 		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.700 0
dbSNP: rs17702471
rs17702471 		0.925 0.120 13 93224864 upstream gene variant A/G snv 0.16
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs17702471
rs17702471 		0.925 0.120 13 93224864 upstream gene variant A/G snv 0.16
CUI: C0677886
Disease: Epithelial ovarian cancer
Epithelial ovarian cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2015 2015