CCRL2, C-C motif chemokine receptor like 2, 9034

N. diseases: 59; N. variants: 3
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: rs1015164
rs1015164
0.925 3 46410189 intron variant A/C;G;T snv
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.700 1.000 2 2015 2019
dbSNP: rs1015164
rs1015164
0.925 3 46410189 intron variant A/C;G;T snv
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
0.700 1.000 2 2015 2019
dbSNP: rs1015164
rs1015164
0.925 3 46410189 intron variant A/C;G;T snv
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.700 1.000 2 2015 2019
dbSNP: rs1015164
rs1015164
0.925 3 46410189 intron variant A/C;G;T snv
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 1.000 2 2015 2019
dbSNP: rs1015164
rs1015164
0.925 3 46410189 intron variant A/C;G;T snv
CUI: C0376705
Disease: Viral Load result
Viral Load result
0.700 1.000 1 2019 2019
dbSNP: rs1015164
rs1015164
0.925 3 46410189 intron variant A/C;G;T snv
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection
0.700 1.000 1 2015 2015
dbSNP: rs6808835
rs6808835
1.000 0.080 3 46408373 synonymous variant G/A;T snv 0.13
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs1015164
rs1015164
0.925 3 46410189 intron variant A/C;G;T snv
CUI: C0019693
Disease: HIV Infections
HIV Infections
Infections; Immune System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1015164
rs1015164
0.925 3 46410189 intron variant A/C;G;T snv
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes
Immune System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs3204849
rs3204849
1.000 0.080 3 46408579 missense variant T/A snv 0.38 0.31
CUI: C1535939
Disease: Pneumocystis jiroveci pneumonia
Pneumocystis jiroveci pneumonia
Infections; Respiratory Tract Diseases 0.010 1.000 1 2011 2011