CEP68, centrosomal protein 68, 23177

N. diseases: 13; N. variants: 6
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: rs2540949
rs2540949 		1.000 0.080 2 65057097 intron variant A/T snv 0.39
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 3 2017 2018
dbSNP: rs2540948
rs2540948 		2 65057489 intron variant T/C snv 0.33
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2015 2018
dbSNP: rs111524356
rs111524356 		2 65057022 intron variant -/GTGGATGCAGCAG;TGGATGCAGCAG;TGGATGCGGCAG;TGTATGCAGCAG delins 0.45
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs111524356
rs111524356 		2 65057022 intron variant -/GTGGATGCAGCAG;TGGATGCAGCAG;TGGATGCGGCAG;TGTATGCAGCAG delins 0.45
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs2249105
rs2249105 		2 65060762 intron variant A/G snv 0.40
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2249105
rs2249105 		2 65060762 intron variant A/G snv 0.40
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2249105
rs2249105 		2 65060762 intron variant A/G snv 0.40
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs2249105
rs2249105 		2 65060762 intron variant A/G snv 0.40
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2249105
rs2249105 		2 65060762 intron variant A/G snv 0.40
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs6728523
rs6728523 		2 65055574 intron variant G/C snv 0.29
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7572857
rs7572857 		0.925 0.160 2 65069664 missense variant G/A snv 0.16 0.12
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: rs7572857
rs7572857 		0.925 0.160 2 65069664 missense variant G/A snv 0.16 0.12
CUI: C0004059
Disease: aspirin intolerance
aspirin intolerance 		0.020 1.000 2 2010 2014
dbSNP: rs7572857
rs7572857 		0.925 0.160 2 65069664 missense variant G/A snv 0.16 0.12
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2014 2014