SDC3, syndecan 3, 9672

N. diseases: 30; 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: rs4949324
rs4949324
1 30904896 intron variant G/A;C snv 0.70
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs2282440
rs2282440
0.882 0.240 1 30874473 missense variant G/A;C snv 9.3E-02
CUI: C4016383
Disease: OBESITY, ASSOCIATION WITH
OBESITY, ASSOCIATION WITH
0.700 0
dbSNP: rs2491132
rs2491132
0.925 0.240 1 30876800 missense variant C/A;G;T snv 8.3E-06; 0.15
CUI: C4016383
Disease: OBESITY, ASSOCIATION WITH
OBESITY, ASSOCIATION WITH
0.700 0
dbSNP: rs2282440
rs2282440
0.882 0.240 1 30874473 missense variant G/A;C snv 9.3E-02
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.040 1.000 4 2006 2018
dbSNP: rs2282440
rs2282440
0.882 0.240 1 30874473 missense variant G/A;C snv 9.3E-02
CUI: C0206081
Disease: Hyperandrogenism
Hyperandrogenism
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs2282440
rs2282440
0.882 0.240 1 30874473 missense variant G/A;C snv 9.3E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2491132
rs2491132
0.925 0.240 1 30876800 missense variant C/A;G;T snv 8.3E-06; 0.15
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2006 2006
dbSNP: rs2491132
rs2491132
0.925 0.240 1 30876800 missense variant C/A;G;T snv 8.3E-06; 0.15
CUI: C0206081
Disease: Hyperandrogenism
Hyperandrogenism
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs4949184
rs4949184
1.000 0.080 1 30874552 missense variant C/A;T snv 1.2E-05; 0.19
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2006 2006