CCR5AS, CCR5 antisense RNA, 102724297

N. diseases: 9; N. variants: 19
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: rs1799987
rs1799987 		0.763 0.200 3 46370444 intron variant A/G snv 0.49
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.020 1.000 2 2011 2018
dbSNP: rs1799987
rs1799987 		0.763 0.200 3 46370444 intron variant A/G snv 0.49
CUI: C1277187
Disease: Left ventricular systolic dysfunction
Left ventricular systolic dysfunction 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1799987
rs1799987 		0.763 0.200 3 46370444 intron variant A/G snv 0.49
CUI: C0014057
Disease: Japanese Encephalitis
Japanese Encephalitis 		Infections; Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1799987
rs1799987 		0.763 0.200 3 46370444 intron variant A/G snv 0.49
CUI: C0745744
Disease: End Stage Liver Disease
End Stage Liver Disease 		Digestive System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1799987
rs1799987 		0.763 0.200 3 46370444 intron variant A/G snv 0.49
CUI: C0343804
Disease: Chronic Chagas' disease
Chronic Chagas' disease 		Infections 0.010 1.000 1 2015 2015
dbSNP: rs1799987
rs1799987 		0.763 0.200 3 46370444 intron variant A/G snv 0.49
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2018 2018
dbSNP: rs1799987
rs1799987 		0.763 0.200 3 46370444 intron variant A/G snv 0.49
CUI: C3887641
Disease: Recurrent hepatitis
Recurrent hepatitis 		Digestive System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1799987
rs1799987 		0.763 0.200 3 46370444 intron variant A/G snv 0.49
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
Cervical Intraepithelial Neoplasia 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1799987
rs1799987 		0.763 0.200 3 46370444 intron variant A/G snv 0.49
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1800023
rs1800023 		1.000 0.040 3 46370817 intron variant A/G snv 0.29
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
Cervical Intraepithelial Neoplasia 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1800023
rs1800023 		1.000 0.040 3 46370817 intron variant A/G snv 0.29
CUI: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms 		Neoplasms; Hemic and Lymphatic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1799987
rs1799987 		0.763 0.200 3 46370444 intron variant A/G snv 0.49
CUI: C4016730
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, DELAYED PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, DELAYED PROGRESSION TO 		0.700 0
dbSNP: rs1001007
rs1001007 		0.827 0.120 3 46387167 intron variant A/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1001007
rs1001007 		0.827 0.120 3 46387167 intron variant A/G;T snv
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1001007
rs1001007 		0.827 0.120 3 46387167 intron variant A/G;T snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1001007
rs1001007 		0.827 0.120 3 46387167 intron variant A/G;T snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1001007
rs1001007 		0.827 0.120 3 46387167 intron variant A/G;T snv
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		Musculoskeletal Diseases 0.700 1.000 1 2016 2016
dbSNP: rs147879075
rs147879075 		1.000 3 46373902 stop gained C/A;G;T snv 1.6E-05; 8.2E-06; 4.1E-06
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection 		0.010 1.000 1 2015 2015
dbSNP: rs1799988
rs1799988 		1.000 0.040 3 46370768 intron variant C/T snv 0.49
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
Cervical Intraepithelial Neoplasia 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1800024
rs1800024 		0.925 0.080 3 46371068 intron variant C/T snv 0.13
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
Cervical Intraepithelial Neoplasia 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1800024
rs1800024 		0.925 0.080 3 46371068 intron variant C/T snv 0.13
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris 		Skin and Connective Tissue Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3087253
rs3087253 		3 46377198 intron variant C/T snv 0.62
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs41469351
rs41469351 		1.000 3 46370771 intron variant C/T snv 6.1E-02
CUI: C4017844
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, INCREASED PERINATAL TRANSMISSION OF
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, INCREASED PERINATAL TRANSMISSION OF 		0.700 0
dbSNP: rs1800452
rs1800452 		3 46373570 missense variant G/A snv 4.9E-03 1.9E-03
CUI: C0019693
Disease: HIV Infections
HIV Infections 		Infections; Immune System Diseases 0.010 1.000 1 2005 2005
dbSNP: rs183662584
rs183662584 		1.000 3 46373218 missense variant G/A snv 5.2E-04 1.5E-04
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection 		0.010 1.000 1 2004 2004