THADA, THADA armadillo repeat containing, 63892

N. diseases: 47; N. variants: 49
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: rs10203174
rs10203174
1.000 0.080 2 43462891 intron variant C/T snv 0.17
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs17030845
rs17030845
2 43460740 intron variant C/T snv 0.11
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 1 2011 2011
dbSNP: rs10179648
rs10179648
1.000 0.120 2 43580926 intron variant C/T snv 0.70
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1038822
rs1038822
1.000 0.120 2 43511034 intron variant T/A;C snv
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs113542380
rs113542380
2 43237679 intron variant G/A snv 4.7E-02
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs113542380
rs113542380
2 43237679 intron variant G/A snv 4.7E-02
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs113542380
rs113542380
2 43237679 intron variant G/A snv 4.7E-02
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs113542380
rs113542380
2 43237679 intron variant G/A snv 4.7E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2016 2016
dbSNP: rs11694173
rs11694173
0.827 0.080 2 43363760 intron variant G/A snv 0.14
CUI: C2678038
Disease: Alopecia, Androgenetic, 2
Alopecia, Androgenetic, 2
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11694173
rs11694173
0.827 0.080 2 43363760 intron variant G/A snv 0.14
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
Alopecia, Androgenetic, 1
0.700 1.000 1 2016 2016
dbSNP: rs11694173
rs11694173
0.827 0.080 2 43363760 intron variant G/A snv 0.14
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11694173
rs11694173
0.827 0.080 2 43363760 intron variant G/A snv 0.14
CUI: C2676272
Disease: Alopecia, Androgenetic, 3
Alopecia, Androgenetic, 3
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11694173
rs11694173
0.827 0.080 2 43363760 intron variant G/A snv 0.14
CUI: C0029489
Disease: Other alopecia
Other alopecia
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11694173
rs11694173
0.827 0.080 2 43363760 intron variant G/A snv 0.14
CUI: C0162311
Disease: Androgenetic Alopecia
Androgenetic Alopecia
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11694173
rs11694173
0.827 0.080 2 43363760 intron variant G/A snv 0.14
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs11891936
rs11891936
1.000 0.120 2 43305163 intron variant C/T snv 0.18
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs11899863
rs11899863
1.000 0.080 2 43391680 intron variant C/T snv 8.5E-02
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs13035011
rs13035011
1.000 0.080 2 43316978 intron variant C/T snv 0.20
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases 0.700 1.000 1 2012 2012
dbSNP: rs13405158
rs13405158
1.000 0.080 2 43478147 intron variant T/C snv 0.17
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs13414381
rs13414381
1.000 0.080 2 43340079 intron variant T/C snv 0.18
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1465618
rs1465618
0.882 0.160 2 43326810 intron variant T/C snv 0.80
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2010 2010
dbSNP: rs17030684
rs17030684
1.000 0.120 2 43320989 intron variant G/A snv 0.19
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs17334919
rs17334919
1.000 0.080 2 43480246 intron variant C/T snv 7.0E-02
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1873555
rs1873555
1.000 0.120 2 43552526 intron variant T/C snv 0.34
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs202032561
rs202032561
2 43520715 intron variant C/T snv 0.11
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018