ANKRD27, ankyrin repeat domain 27, 84079

N. diseases: 7; 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: rs17692896
rs17692896 		1.000 0.040 19 32598525 intron variant G/A snv 4.6E-02
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.800 1.000 1 2013 2013
dbSNP: rs34540877
rs34540877 		19 32599365 intron variant T/C snv 2.0E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 2 2016 2017
dbSNP: rs34540877
rs34540877 		19 32599365 intron variant T/C snv 2.0E-02
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 2 2016 2017
dbSNP: rs2903754
rs2903754 		0.925 0.200 19 32600776 intron variant C/T snv 0.62
CUI: C0343386
Disease: Clostridium difficile infection
Clostridium difficile infection 		Infections 0.700 1.000 1 2018 2018
dbSNP: rs2903754
rs2903754 		0.925 0.200 19 32600776 intron variant C/T snv 0.62
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs35946544
rs35946544 		19 32619077 intron variant C/T snv 0.40
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs3815700
rs3815700 		1.000 0.120 19 32602346 intron variant T/C snv 0.19
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis 		Digestive System Diseases; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2014 2014
dbSNP: rs749927570
rs749927570 		19 32676628 missense variant C/G;T snv 7.9E-05
CUI: C1842073
Disease: Prolonged Electroretinal Response Suppression
Prolonged Electroretinal Response Suppression 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0