rs1799987, CCR5AS;CCR5

N. diseases: 10
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.
ACQUIRED IMMUNODEFICIENCY SYNDROME, DELAYED PROGRESSION TO
CUI: C4016730
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, DELAYED PROGRESSION TO
1 0.763 0.200 3 46370444 intron variant A/G snv 0.49 0.700 0
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.763 0.200 3 46370444 intron variant A/G snv 0.49 0.020 1.000 2 2011 2018
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.763 0.200 3 46370444 intron variant A/G snv 0.49 0.010 1.000 1 2012 2012
Cervical Intraepithelial Neoplasia
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
29 0.763 0.200 3 46370444 intron variant A/G snv 0.49 0.010 1.000 1 2019 2019
Chronic Chagas' disease
CUI: C0343804
Disease: Chronic Chagas' disease
4 0.763 0.200 3 46370444 intron variant A/G snv 0.49 0.010 1.000 1 2015 2015
End Stage Liver Disease
CUI: C0745744
Disease: End Stage Liver Disease
3 0.763 0.200 3 46370444 intron variant A/G snv 0.49 0.010 1.000 1 2011 2011
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.763 0.200 3 46370444 intron variant A/G snv 0.49 0.010 1.000 1 2018 2018
Japanese Encephalitis
CUI: C0014057
Disease: Japanese Encephalitis
6 0.763 0.200 3 46370444 intron variant A/G snv 0.49 0.010 1.000 1 2019 2019
Left ventricular systolic dysfunction
CUI: C1277187
Disease: Left ventricular systolic dysfunction
11 0.763 0.200 3 46370444 intron variant A/G snv 0.49 0.010 1.000 1 2015 2015
Recurrent hepatitis
CUI: C3887641
Disease: Recurrent hepatitis
5 0.763 0.200 3 46370444 intron variant A/G snv 0.49 0.010 1.000 1 2011 2011