SOCS2, suppressor of cytokine signaling 2, 8835

N. diseases: 104; N. variants: 8
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: rs11107116
rs11107116 		1.000 0.080 12 93584728 downstream gene variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2008 2019
dbSNP: rs11107116
rs11107116 		1.000 0.080 12 93584728 downstream gene variant G/A;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2008 2010
dbSNP: rs3825199
rs3825199 		12 93583178 3 prime UTR variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2008 2014
dbSNP: rs9634212
rs9634212 		12 93599490 intergenic variant C/A snv 0.19
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2017 2019
dbSNP: rs10492321
rs10492321 		12 93586312 downstream gene variant T/A snv 0.20
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2013 2013
dbSNP: rs10492321
rs10492321 		12 93586312 downstream gene variant T/A snv 0.20
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs10859536
rs10859536 		12 93595956 intergenic variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs11107116
rs11107116 		1.000 0.080 12 93584728 downstream gene variant G/A;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11107120
rs11107120 		12 93591706 intergenic variant T/C snv 0.19
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1316739
rs1316739 		12 93574480 3 prime UTR variant G/A snv 0.26
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs3782415
rs3782415 		0.925 0.280 12 93573979 3 prime UTR variant T/C snv 0.20
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs3825199
rs3825199 		12 93583178 3 prime UTR variant A/G;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs3782415
rs3782415 		0.925 0.280 12 93573979 3 prime UTR variant T/C snv 0.20
CUI: C0041408
Disease: Turner Syndrome
Turner Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs3782415
rs3782415 		0.925 0.280 12 93573979 3 prime UTR variant T/C snv 0.20
CUI: C0271561
Disease: Somatotropin deficiency
Somatotropin deficiency 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases 0.010 1.000 1 2014 2014