PDGFD, platelet derived growth factor D, 80310

N. diseases: 94; N. variants: 7
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: rs10895596
rs10895596 		11 104161315 intron variant G/A snv 0.29
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11226158
rs11226158 		1.000 0.040 11 104107399 intron variant C/A;G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11226159
rs11226159 		1.000 0.040 11 104107812 intron variant T/G snv 0.24
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12274248
rs12274248 		11 103954382 intron variant C/T snv 4.2E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12274248
rs12274248 		11 103954382 intron variant C/T snv 4.2E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7950273
rs7950273 		0.925 0.120 11 104160870 intron variant C/G snv 0.32
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7950273
rs7950273 		0.925 0.120 11 104160870 intron variant C/G snv 0.32
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.020 0.500 2 2008 2016
dbSNP: rs3809021
rs3809021 		0.882 0.080 11 104164894 upstream gene variant T/G snv 0.61
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs3809021
rs3809021 		0.882 0.080 11 104164894 upstream gene variant T/G snv 0.61
CUI: C0795687
Disease: Cerebral arterial thrombosis
Cerebral arterial thrombosis 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs3809021
rs3809021 		0.882 0.080 11 104164894 upstream gene variant T/G snv 0.61
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs3809021
rs3809021 		0.882 0.080 11 104164894 upstream gene variant T/G snv 0.61
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs591118
rs591118 		1.000 0.080 11 104095993 intron variant A/G snv 0.55
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs7950273
rs7950273 		0.925 0.120 11 104160870 intron variant C/G snv 0.32
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs7950273
rs7950273 		0.925 0.120 11 104160870 intron variant C/G snv 0.32
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs7950273
rs7950273 		0.925 0.120 11 104160870 intron variant C/G snv 0.32
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2008 2008