rs2075800, HSPA1L

N. diseases: 8
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 0.700 1.000 3 2007 2011
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 0.700 1.000 1 2010 2010
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 0.700 1.000 1 2015 2015
Idiopathic Pulmonary Fibrosis
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
63 0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 0.010 1.000 1 2015 2015
Paranoid Schizophrenia
CUI: C0036349
Disease: Paranoid Schizophrenia
23 0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 0.010 1.000 1 2018 2018
Sarcoidosis
CUI: C0036202
Disease: Sarcoidosis
787 0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 0.010 1.000 1 2007 2007
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
38 0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 0.010 1.000 1 2012 2012
Uveitis
CUI: C0042164
Disease: Uveitis
43 0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 0.010 1.000 1 2007 2007